0000000001299030
AUTHOR
Edwin C. Constable
showing 141 related works from this author
Inside Front Cover: Long-Living Light-Emitting Electrochemical Cells - Control through Supramolecular Interactions (Adv. Mater. 20/2008)
2008
Efficient Green Light-Emitting Electrochemical Cells Based on Ionic Iridium Complexes with Sulfone-Containing Cyclometalating Ligands
2013
A new approach to obtain green-emitting iridiumA complexes is described. The synthetic approach consists of introducing a methylsulfone electron-withdrawing substituent into a 4-phenylpyrazole cyclometalating ligand in order to stabilize the highest- occupied molecular orbital (HOMO). Six new complexes have been synthe- sized incorporating the conjugate base of 1-(4-(methylsulfonyl)phenyl)-1 H- pyrazole as the cyclometalating ligand. The complexes show green emission and very high photoluminescence quantum yields in both diluted and concentrated films. When used as the main active component in light-emit- ting electrochemical cells (LECs), green electroluminance is observed. High efficienci…
Thienylpyridine-based cyclometallated iridium(III) complexes and their use in solid state light-emitting electrochemical cells
2013
The synthesis and characterization of four iridium(iii) complexes [Ir(thpy)2(N^N)][PF6] where Hthpy = 2-(2'-thienyl)pyridine and N^N are 6-phenyl-2,2'-bipyridine (1), 4,4'-di-(t)butyl-2,2'-bipyridine (2), 4,4'-di-(t)butyl-6-phenyl-2,2'-bipyridine (3) or 4,4'-dimethylthio-2,2'-bipyridine (4) are described. The single crystal structures of ligand 4 and the complexes containing the [Ir(thpy)2(1)](+) and [Ir(thpy)2(4)](+) cations have been determined. In [Ir(thpy)2(1)](+), the pendant phenyl ring engages in an intra-cation π-stacking interaction with one of the thienyl rings in the solid state, and undergoes hindered rotation on the NMR timescale in [Ir(thpy)2(1)](+) and [Ir(thpy)2(3)](+). The …
Solution, structural and photophysical aspects of substituent effects in the N^N ligand in [Ir(C^N)2(N^N)]+ complexes
2013
The syntheses and properties of a series of eleven new [Ir(ppy)2(N^N)][PF6] complexes (Hppy = 2-phenylpyridine) are reported. The N^N ligands are based on 2,2-bipyridine (bpy), substituted in the 6- or 5-positions with groups that are structurally and electronically diverse. All but two of the N^N ligands incorporate an aromatic ring, designed to facilitate intra-cation face-to-face π-interactions between the N^N and one [ppy](-) ligand. Within the set of ligands, 6-(3-tolyl)-2,2'-bipyridine (5), 4,6-bis(4-nitrophenyl)-2,2'-bipyridine (9), and 4,6-bis(3,4,5-trimethoxyphenyl)-2,2'-bipyridine (10) are new and their characterization includes single crystal structures of 9, and two polymorphs o…
Bright and stable light-emitting electrochemical cells based on an intramolecularly π-stacked, 2-naphthyl-substituted iridium complex
2014
The synthesis and characterization of a new cationic bis-cyclometallated iridium(III) complex and its use in solid-state light-emitting electrochemical cells (LECs) are described. The complex [Ir(ppy)2(Naphbpy)][PF6], where Hppy = 2-phenylpyridine and Naphbpy = 6-(2-naphthyl)-2,2′-bipyridine, incorporates a pendant 2-naphthyl unit that π-stacks face-to-face with the adjacent ppy− ligand and acts as a peripheral bulky group. The complex presents a structureless emission centred around 595–600 nm both in solution and in thin film with relatively low photoluminescence quantum yields compared with analogous systems. Density functional theory calculations support the charge transfer character of…
Highly Stable Red-Light-Emitting Electrochemical Cells
2017
The synthesis and characterization of a series of new cyclometalated iridium(III) complexes [Ir(ppy) 2 (N ∧ N)][PF 6 ] in which Hppy = 2-phenylpyridine and N ∧ N is (pyridin-2-yl)benzo[ d ]thiazole ( L1 ), 2-(4-( tert -butyl)pyridin-2-yl)benzo[ d ]thiazole ( L2 ), 2-(6-phenylpyridin-2-yl)benzo[ d ]thiazole ( L3 ), 2-(4-( tert -butyl)-6-phenylpyridin-2-yl)benzo[ d ]thiazole ( L4 ), 2,6-bis(benzo[ d ]thiazol-2-yl)pyridine ( L5 ), 2-(pyridin-2-yl)benzo[ d ]oxazole ( L6 ), or 2,2′-dibenzo[ d ]thiazole ( L7 ) are reported. The single crystal structures of [Ir(ppy) 2 ( L1 )][PF 6 ]·1.5CH 2 Cl 2 , [Ir(ppy) 2 ( L6 )][PF 6 ]·CH 2 Cl 2 , and [Ir(ppy) 2 ( L7 )][PF 6 ] have been determined. The new com…
[Ir(C^N)2(N^N)]+ emitters containing a naphthalene unit within a linker between the two cyclometallating ligands
2016
The synthesis of four cyclometallated [Ir(C^N) 2 (N^N)][PF 6 ] compounds in which N^N is a substituted 2,2’- -bipyridine (bpy) ligand and the naphthyl-centred ligand 2,7-bis(2-(2-(4-(pyridin-2-yl)phenoxy)ethoxy) ethoxy)naphthalene provides the two cyclometallating C^N units is reported. The iridium( III ) complexes have been characterized by 1 H and 13 C NMR spectroscopies, mass spectrometry and elemental analysis, and their electrochemical and photophysical properties are described. Comparisons are made with a model [Ir(ppy) 2 (N^N)][PF 6 ] compound (Hppy = 2-phenylpyridine). The complexes containing the naphthyl-unit exhibit similar absorption spectra and excitation at 280 nm leads to an …
Efficient and Long-Living Light-Emitting Electrochemical Cells
2010
Three new heteroleptic iridium complexes that combine two approaches, one leading to a high stability and the other yielding a high luminescence efficiency, are presented. All complexes contain a phenyl group at the 6-position of the neutral bpy ligand, which holds an additional, increasingly bulky substituent on the 4-position. The phenyl group allows for intramolecular π–π stacking, which renders the complex more stable and yields long-living light-emitting electrochemical cells (LECs). The additional substituent increases the intersite distance between the cations in the film, reducing the quenching of the excitons, and should improve the efficiency of the LECs. Density functional theory…
A Supramolecularly-Caged Ionic Iridium(III) Complex Yielding Bright and Very Stable Solid-State Light-Emitting Electrochemical Cells
2008
A new iridium(III) complex showing intramolecular interligand pi-stacking has been synthesized and used to improve the stability of single-component, solid-state light-emitting electrochemical cell (LEC) devices. The pi-stacking results in the formation of a very stable supramolecularly caged complex. LECs using this complex show extraordinary stabilities (estimated lifetime of 600 h) and luminance values (average luminance of 230 cd m-2) indicating the path toward stable ionic complexes for use in LECs reaching stabilities required for practical applications.
Remote Modification of Bidentate Phosphane Ligands Controlling the Photonic Properties in Their Complexes: Enhanced Performance of [Cu(RN‐xantphos)(N…
2020
A series of copper(I) complexes of the type [Cu(HN-xantphos)(N^N)][PF6] and [Cu(BnN-xantphos)(N^N)][PF6], in which N^N = bpy, Mebpy and Me2bpy, HN-xantphos = 4,6-bis(diphenylphosphanyl)-10H-phenoxazine and BnN-xantphos = 10-benzyl-4,6-bis(diphenylphosphanyl)-10H-phenoxazine is described. The single crystal structures of [Cu(HN-xantphos)(Mebpy)][PF6] and [Cu(BnN-xantphos)(Me2bpy)][PF6] confirm the presence of N^N and P^P chelating ligands with the copper(I) atoms in distorted coordination environments. Solution electrochemical and photophysical properties of the BnN-xantphos-containing compounds (for which the highest-occupied molecular orbital is located on the phenoxazine moiety) are repor…
Modulation of the solubility of luminescent semiconductor nanocrystals through facile surface functionalization
2014
The solubility of luminescent quantum dots in solvents from hexane to water can be finely tuned by the choice of the countercations associated with carboxylate residues present on the nanocrystal surface. The resulting nanocrystals exhibit long term colloidal and chemical stability and maintain their photophysical properties.
Regioisomerism in cationic sulfonyl-substituted [Ir(C^N)2(N^N)]+ complexes: its influence on photophysical properties and LEC performance
2016
A series of regioisomeric cationic iridium complexes of the type [Ir(C^N)2(bpy)][PF6] (bpy = 2,2'-bipyridine) is reported. The complexes contain 2-phenylpyridine-based cyclometallating ligands with a methylsulfonyl group in either the 3-, 4- or 5-position of the phenyl ring. All the complexes have been fully characterized, including their crystal structures. In acetonitrile solution, all the compounds are green emitters with emission maxima between 493 and 517 nm. Whereas substitution meta to the Ir-C bond leads to vibrationally structured emission profiles and photoluminescence quantum yields of 74 and 77%, placing a sulfone substituent in a para position results in a broad, featureless em…
Colour tuning by the ring roundabout: [Ir(C^N)2(N^N)]+ emitters with sulfonyl-substituted cyclometallating ligands
2015
A series of cationic bis-cyclometallated iridium(III) complexes [Ir(C^N)2(N^N)]+ is reported. Cyclometallating C^N ligands are based on 2-phenylpyridine with electron-withdrawing sulfone substituents in the phenyl ring: 2-(4-methylsulfonylphenyl)pyridine (H1) and 2-(3-methylsulfonylphenyl)pyridine (H2). 2-(1H-Pyrazol-1-yl)pyridine (pzpy) and 2-(3,5-dimethyl-1H-pyrazol-1-yl)pyridine (dmpzpy) are used as electron-rich ancillary N^N ligands. The complexes have been fully characterized and the single crystal structure of [Ir(2)2(dmpzpy)][PF6]·MeCN has been determined. Depending on the position of the methylsulfonyl group, the complexes are green or blue emitters with vibrationally structured em…
Light-emitting electrochemical cells based on a supramolecularly-caged phenanthroline-based iridium complex.
2011
The complex [Ir(ppy)(2)(pphen)][PF(6)] (Hppy = 2-phenylpyridine, pphen = 2-phenyl-1,10-phenanthroline) has been prepared and evaluated as an electroluminescent component for light-emitting electrochemical cells (LECs). Like in analogous LECs using bpy-based iridium(III) complexes a significant enhancement of the device stability is observed.
Shine bright or live long: substituent effects in [Cu(N^N)(P^P)]+-based light-emitting electrochemical cells where N^N is a 6-substituted 2,2'-bipyri…
2016
We report [Cu(P^P)(N^N)][PF6] complexes with P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 6-methyl-2,2′-bipyridine (Mebpy), 6-ethyl-2,2′-bipyridine (Etbpy), 6,6′-dimethyl-2,2′-bipyridine (Me2bpy) or 6-phenyl-2,2′-bipyridine (Phbpy). The crystal structures of [Cu(POP)(Phbpy)][PF6]·Et2O, [Cu(POP)(Etbpy)][PF6]·Et2O, [Cu(xantphos)(Me2bpy)][PF6], [Cu(xantphos)(Mebpy)][PF6]·CH2Cl2·0.4Et2O, [Cu(xantphos)(Etbpy)][PF6]·CH2Cl2·1.5H2O and [Cu(xantphos)(Phbpy)][PF6] are described; each copper(I) centre is distorted tetrahedral. In the crystallographically determined structures, the N^N domain in [Cu(xantphos)(Phbpy)]+ and [Cu(…
Copper(i) complexes for sustainable light-emitting electrochemical cells
2011
Four prototype heteroleptic copper(I) complexes [Cu(bpy)(pop)][PF6] (bpy = 2,2′-bipyridine, pop = bis(2-(diphenylphosphino)phenyl)ether), [Cu(phen)(pop)][PF6] (phen = 1,10-phenanthroline), [Cu(bpy)(pdpb)][PF6] (pdpb = 1,2-bis(diphenylphosphino)benzene) and [Cu(phen)(pdpb)][PF6] are presented. The synthesis, X-ray structures, solution and solid-state photophysical studies, and the performance in light-emitting electrochemical cells (LECs) of these complexes are described. Their photophysical properties are interpreted with the help of density functional theory (DFT) calculations. The photophysical studies in solution and in the solid-state indicate that these copper(I) complexes show good lu…
Red emitting [Ir(C^N)2(N^N)]+ complexes employing bidentate 2,2':6,2''-terpyridine ligands for light-emitting electrochemical cells
2014
2,2':6',2''-Terpyridine (tpy), 4'-(4-HOC6H4)-2,2':6',2''-terpyridine (1), 4'-(4-MeOC6H4)-2,2':6',2''-terpyridine (2), 4'-(4-MeSC6H4)-2,2':6',2''-terpyridine (3), 4'-(4-H2NC6H4)-2,2':6',2''-terpyridine (4) and 4'-(4-pyridyl)-2,2':6',2''-terpyridine (4) act as N^N chelates in complexes of the type [Ir(C^N)2(N^N)][PF6] in which the cyclometallating ligand, C^N, is derived from 2-phenylpyridine (Hppy) or 3,5-dimethyl-1-phenyl-1H-pyrazole (Hdmppz). The single crystal structures of eight complexes have been determined, and in each iridium(III) complex cation, the non-coordinated pyridine ring of the tpy unit is involved in a face-to-face π-stacking interaction with the cyclometallated ring of an …
Low Current Density Driving Leads to Efficient, Bright and Stable Green Electroluminescence
2013
Electroluminescent devices have the potential to reshape lighting and display technologies by providing low-energy consuming solutions with great aesthetic features, such as flexibility and transparency. In particular, light-emitting electrochemical cells (LECs) are among the simplest electro-luminescent devices. The device operates with air-stable materials and the active layer can be resumed to an ionic phosphorescent emitter. As a consequence, LECs can be assembled using solution-process technologies, which could allow for low-cost and large-area lighting applications in the future. High efficiencies have been reported at rather low luminances (<50 cd m(-2)) and at very low current densi…
Exploring the effect of the cyclometallating ligand in 2-(pyridine-2-yl)benzo[d]thiazole-containing iridium(III) complexes for stable light-emitting …
2018
The preparation and characterization of a series of iridium(III) ionic transition-metal complexes for application in light-emitting electrochemical cells (LECs) are reported. The complexes are of the type [Ir(C^N)2(N^N)][PF6] in which C^N is one of the cyclometallating ligands 2-(3-(tert-butyl)phenyl)pyridine (tppy), 2-phenylbenzo[d]thiazole (pbtz), 1-phenyl-1H-pyrazole (ppz) and 1-phenylisoquninoline (piq), and N^N is 2-(pyridine-2-yl)benzo[d]thiazole (btzpy). The variation in the C^N ligands allows the HOMO energy level to be tuned, leading to HOMO–LUMO gaps in the range 2.76–3.01 eV and values of Eox1/2 of 0.81–1.11 V. In solution, the complexes are orange to deep-red emitters (λmax in t…
Peripheral halo-functionalization in [Cu(N^N)(P^P)]+ emitters: influence on the performances of light-emitting electrochemical cells
2016
A series of heteroleptic [Cu(N^N)(P^P)][PF6] complexes is described in which P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 4,4′-diphenyl-6,6′-dimethyl-2,2′-bipyridine substituted in the 4-position of the phenyl groups with atom X (N^N = 1 has X = F, 2 has X = Cl, 3 has X = Br, 4 has X = I; the benchmark N^N ligand with X = H is 5). These complexes have been characterized by multinuclear NMR spectroscopy, mass spectrometry, elemental analyses and cyclic voltammetry; representative single crystal structures are also reported. The solution absorption spectra are characterized by high energy bands (arising from ligand-c…
Long-Living Light-Emitting Electrochemical Cells - Control through Supramolecular Interactions
2008
Light-emitting electrochemical cells with lifetimes surpassing 3000 hours at an average luminance of 200 cd m(-2) are obtained with an ionic iridium(III) complex conveniently designed to form a supramolecularly caged structure.
A counterion study of a series of [Cu(P^P)(N^N)][A] compounds with bis(phosphane) and 6-methyl and 6,6′-dimethyl-substituted 2,2′-bipyridine ligands …
2021
The syntheses and characterisations of a series of heteroleptic copper(i) compounds [Cu(POP)(Mebpy)][A], [Cu(POP)(Me2bpy)][A], [Cu(xantphos)(Mebpy)][A] and [Cu(xantphos)(Me2bpy)][A] in which [A]− is [BF4]−, [PF6]−, [BPh4]− and [BArF4]− (Mebpy = 6-methyl-2,2′-bipyridine, Me2bpy = 6,6′-dimethyl-2,2′-bipyridine, POP = oxydi(2,1-phenylene)bis(diphenylphosphane), xantphos = (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphane), [BArF4]− = tetrakis(3,5-bis(trifluoromethyl)phenyl)borate) are reported. Nine of the compounds have been characterised by single crystal X-ray crystallography, and the consequences of the different anions on the packing interactions in the solid state are discussed. T…
Dual-Emissive Photoluminescent Langmuir−Blodgett Films of Decatungstoeuropate and an Amphiphilic Iridium Complex
2009
Langmuir monolayers and Langmuir-Blodgett (LB) films of the decatungstoeuropate [Eu(W(5)O(18))(2)](9-) (EuW(10)) and the amphiphilic Ir complex 1 have been successfully fabricated by using the adsorption properties of the EuW(10) polyanion dissolved in the aqueous subphase onto a positively charged 1 monolayer at the air-water interface. The compression isotherms and Brewster angle microscopy (BAM) of monolayers of 1 on pure water (1 monolayer) and on a subphase containing 10(-6) M EuW(10) and 10(-3) M NaCl (1/EuW(10) monolayer) have been studied. Infrared and UV-vis spectroscopy of the transferred LB films indicate that EuW(10) and 1 molecules are incorporated within these LB films. X-ray …
Tuning the photophysical properties of cationic iridium(iii) complexes containing cyclometallated 1-(2,4-difluorophenyl)-1H-pyrazole through function…
2012
Four new heteroleptic iridium(III) complexes in the family [Ir(dfppz)(2)((NN)-N-boolean AND)](+), where Hdfppz = 1-(2,4-difluorophenyl)-1H-pyrazole and (NN)-N-boolean AND = 6-phenyl-2,2'-bipyridine (1), 4,4'-(di-tert-butyl)-6-phenyl-2,2'-bipyridine (2), 4,4'-(di-tert-butyl)-6,6'-diphenyl-2,2'-bipyridine (3) and 4,4'-bis(dimethylamino)-2,2'-bipyridine (4), have been synthesized as the hexafluoridophosphate salts and fully characterized. Single crystal structures of ligand 3 and the precursor [Ir-2(dfppz)(4)(mu-Cl)(2)] have been determined, along with the structures of the complexes 4{[Ir(dfppz)(2)(1)][PF6]}center dot 3CH(2)Cl(2), [Ir(dfppz)(2)(3)][PF6]center dot CH2Cl2 and [Ir(dfppz)(2)(4)][…
Phosphane tuning in heteroleptic [Cu(N^N)(P^P)]+ complexes for light-emitting electrochemical cells
2019
The synthesis and characterization of five [Cu(P^P)(N^N)][PF 6 ] complexes in which P^P = 2,7-bis( tert -butyl)-4,5-bis(diphenylphosphino)-9,9-dimethylxanthene ( t Bu 2 xantphos) or the chiral 4,5-bis(mesitylphenylphosphino)-9,9-dimethylxanthene (xantphosMes 2 ) and N^N = 2,2'-bipyridine (bpy), 6-methyl-2,2'-bipyridine (6-Mebpy) or 6,6'-dimethyl-2,2'-bipyridine (6,6'-Me 2 bpy) are reported. Single crystal structures of four of the compounds confirm that the copper(I) centre is in a distorted tetrahedral environment. In [Cu(xantphosMes 2 )(6-Mebpy)][PF 6 ], the 6-Mebpy unit is disordered over two equally populated orientations and this disorder parallels a combination of two dynamic processe…
Fine‐Tuning of Photophysical and Electronic Properties of Materials for Photonic Devices Through Remote Functionalization
2012
We report four new iridium(III) complexes of the type [Ir(ppy)2(N?N)][PF6] in which N?N is a 4,6-diphenyl-2,2`-bipyridine and the 4-phenyl ring is substituted at either the para or meta positions [4-Me, N?N = 1; 4-Br, N?N = 2; 3,5-Br2, N?N = 3; 3,5-(C6H4-4-NPh2)2, N?N = 4]. The complexes have been fully characterized, and single-crystal diffraction analyses of [Ir(ppy)2(N?N)][PF6] (N?N = 13) confirmed that each [Ir(ppy)2(N?N)]+ cation exhibits face-to-face p-stacking between the pendant phenyl substituent of the N?N ligand and the cyclometallated phenyl ring of an adjacent [ppy] ligand. In solution, the complexes are short-lived emitters; the emission maxima for [Ir(ppy)2(1)][PF6], [Ir(ppy)…
Stable and Efficient Solid-State Light-Emitting Electrochemical Cells Based on a Series of Hydrophobic Iridium Complexes
2011
Light-emitting electrochemical cells (LECs) based on ionic transition-metal complexes (iTMCs) exhibiting high efficiency, short turn-on time, and long stability have recently been presented. Furthermore, LECs emitting in the full range of the visible spectrum including white light have been reported. However, all these achievements were obtained individually, not simultaneously, using in each case a different iTMC. In this work, device stability is maintained by employing intrinsically stable ionic iridium complexes, while increasing the complex and the device quantum yields for exciton-to-photon conversion. This is done by sequentially modifying the archetype ionic iridium complex [Ir(ppy)…
Long-Living Emitting Electrochemical Cells Based on Supramolecular π-π Interactions
2009
AbstractThe complex [Ir(ppy)2(dpbpy)][PF6] (Hppy = 2-phenylpyridine, dpbpy = 6,6'-diphenyl-2,2'-bipyridine) has been prepared and evaluated as an electroluminescent component for light-emitting electrochemical cells (LECs). The complex exhibits two intramolecular face-to-face π-stacking interactions and long-lived LECs have been constructed; the device characteristics are not significantly improved in comparison to analogous LECs with 6-phenyl-2,2'-bipyridine with only one π-stacking interaction.
Luminescent copper(i) complexes with bisphosphane and halogen-substituted 2,2′-bipyridine ligands
2018
Heteroleptic [Cu(P^P)(N^N)][PF6] complexes, where N^N is a halo-substituted 2,2'-bipyridine (bpy) and P^P is either bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9- dimethylxanthene (xantphos) have been synthesized and investigated. To stabilize the tetrahedral geometry of the copper(I) complexes, the steric demands of the bpy ligands have been increased by introducing 6- or 6,6'-halo-substituents in 6,6'-dichloro-2,2'-bipyridine (6,6'-Cl2bpy), 6-bromo-2,2'- bipyridine (6-Brbpy) and 6,6'-dibromo-2,2'-bipyridine (6,6'-Br2bpy). The solid-state structures of [Cu(POP)(6,6'-Cl2bpy)][PF6], [Cu(xantphos)(6,6'-Cl2bpy)][PF6].CH2Cl2, [Cu(POP)(6-Brbpy)][PF6] and [Cu(xantp…
Archetype Cationic Iridium Complexes and Their Use in Solid-State Light-Emitting Electrochemical Cells
2009
The archetype ionic transition-metal complexes (iTMCs) [Ir(ppy)2(bpy)][PF6] and [Ir(ppy)2(phen)][PF6], where Hppy = 2-phenylpyridine, bpy = 2,2'-bipyridine, and phen = 1,10-phenanthroline, are used as the primary active components in light-emitting electrochemical cells (LECs). Solution and solid-state photophysical properties are reported for both complexes and are interpreted with the help of density functional theory calculations. LEC devices based on these archetype complexes exhibit long turn-on times (70 and 160 h, respectively) and low external quantum efficiencies (~ 2%) when the complex is used as a pure film. The long turn-on times are attributed to the low mobility of the counter…
Two are not always better than one: ligand optimisation for long-living light-emitting electrochemical cells
2009
The complex [Ir(ppy)2(dpbpy)][PF6] (Hppy = 2-phenylpyridine, dpbpy = 6,6'-diphenyl-2,2'-bipyridine) has been prepared and evaluated as an electroluminescent component for light-emitting electrochemical cells (LECs); the complex exhibits two intramolecular face-to-face π-stacking interactions and long-lived LECs have been constructed; the device characteristics are not significantly improved in comparison to analogous LECs with 6-phenyl-2,2'-bipyridine. Costa Riquelme, Ruben Dario, Ruben.Costa@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es ; Bolink, Henk, Henk.Bolink@uv.es
Bis-Sulfone- and Bis-Sulfoxide-Spirobifluorenes: Polar Acceptor Hosts with Tunable Solubilities for Blue-Phosphorescent Light-Emitting Devices
2016
Bis-sulfone- and bis-sulfoxide-spirobifluorenes are a promising class of high-triplet-energy electron-acceptor hosts for blue phosphorescent light-emitting devices. The molecular design and synthetic route are simple and facilitate tailoring of the solubilities of the host materials without lowering the high-energy triplet state. The syntheses and characterization (including single-crystal structures) of four electron-accepting hosts are reported; the trend in their reduction potentials is consistent with the electron-withdrawing nature of the sulfone or sulfoxide substituents. Emission maxima of 421–432 nm overlap with the MLCT absorption of the sky-blue emitter bis(4,6-difluorophenyl-pyri…
CF3 Substitution of [Cu(P^P)(bpy)][PF6 ] Complexes: Effects on Photophysical Properties and Light-Emitting Electrochemical Cell Performance
2018
Herein, [Cu(P^P)(N^N)][PF6 ] complexes (P^P=bis[2-(diphenylphosphino)phenyl]ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos); N^N=CF3 -substituted 2,2'-bipyridines (6,6'-(CF3 )2 bpy, 6-CF3 bpy, 5,5'-(CF3 )2 bpy, 4,4'-(CF3 )2 bpy, 6,6'-Me2 -4,4'-(CF3 )2 bpy)) are reported. The effects of CF3 substitution on their structure as well as their electrochemical and photophysical properties are also presented. The HOMO-LUMO gap was tuned by the N^N ligand; the largest redshift in the metal-to-ligand charge transfer (MLCT) band was for [Cu(P^P){5,5'-(CF3 )2 bpy}][PF6 ]. In solution, the compounds are weak yellow to red emitters. The emission properties depend on the substitu…
Intramolecular pi-stacking in a phenylpyrazole-based iridium complex and its use in light-emitting electrochemical cells.
2010
A novel iridium(III) complex, [Ir(dmppz)(2)pbpy][PF(6)] (Hdmppz = 3,5-dimethyl-1-phenylpyrazole and pbpy = 6-phenyl-(2,2'-bipyridine)), is reported. The complex shows an intramolecular face-to-face pi-stacking between the phenyl ring of the dmppz ligand and the pendant phenyl of the pbpy ligand. This interaction provides a supramolecular cage formation that holds also in the excited states. Light-emitting electrochemical cells (LECs) using the novel complex show extraordinary lifetimes of approximately 2000 h. The high stability is favored by the presence of pendant methyl groups on the dmppz ligands that hinder the entrance of water molecules rendering the degradation of the complex more d…
Chloride ion impact on materials for light-emitting electrochemical cells
2013
Small quantities of Cl(-) ions result in dramatic reductions in the performance of ionic transition metal complexes in light-emitting electrochemical cells. Strong ion-pairing between aromatic protons and chloride has been established in both the solid state and solution. X-ray structural determination of 2{[Ir(ppy)2(bpy)][Cl]}·2CH2Cl2·[H3O]·Cl reveals the unusual nature of an impurity encountered in the preparation of [Ir(ppy)2(bpy)][PF6].
[Cu(P^P)(N^N)][PF6] compounds with bis(phosphane) and 6-alkoxy, 6-alkylthio, 6-phenyloxy and 6-phenylthio-substituted 2,2'-bipyridine ligands for lig…
2018
We report a series of [Cu(P^P)(N^N)][PF6] complexes with P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 6-methoxy-2,2′-bipyridine (MeObpy), 6-ethoxy-2,2′-bipyridine (EtObpy), 6-phenyloxy-2,2′-bipyridine (PhObpy), 6-methylthio-2,2′-bipyridine (MeSbpy), 6-ethylthio-2,2′-bipyridine (EtSbpy) and 6-phenylthio-2,2′-bipyridine (PhSbpy). The single crystal structures of all twelve compounds have been determined and confirm chelating modes for each N^N and P^P ligand, and a distorted tetrahedral geometry for copper(I). For the xantphos-containing complexes, the asymmetrical bpy ligand is arranged with the 6-substituent lying …
Single Molecule Solid State Light Emitting Electrochemical Cells with Lifetimes Superior to 3000 Hours
2008
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
2015
A series of cyclometalated iridium(iii) complexes [Ir(C^N)2(N^N)][PF6] (N^N = 2,2′-bipyridine (1), 6-phenyl-2,2′-bipyridine (2), 4,4′-di-tert-butyl-2,2′-bipyridine (3), 4,4′-di-tert-butyl-6-phenyl-2,2′-bipyridine (4); HC^N = 2-(3-phenyl)phenylpyridine (HPhppy) or 2-(3,5-diphenyl)phenylpyridine (HPh2ppy)) are reported. They have been synthesized using solvento precursors so as to avoid the use of chlorido-dimer intermediates, chloride ion contaminant being detrimental to the performance of [Ir(C^N)2(N^N)][PF6] emitters in light-electrochemical cell (LEC) devices. Single crystal structure determinations and variable temperature solution 1H NMR spectroscopic data confirm that the pendant pheny…
Not just size and shape: spherically symmetrical d5 and d10 metal ions give different coordination nets with 4,2′:6′,4″-terpyridines
2010
Functionalized 4,2′:6′,4″-terpyridine ligands have been used to provide a divergent N,N′-donor set for the formation of coordination polymers containing {Zn2(µ-OAc)4} or {Mn3(µ-OAc)4(OAc)2} scaffolds. Single-stranded coordination polymers are produced from the reactions of 4′-(4-bromophenyl)-4,2′:6′,4″-terpyridine (1) and 4′-(4-methylthiophenyl)-4,2′:6′,4″-terpyridine (2) with Zn(OAc)2·2H2O. In [Zn2(1)(OAc)4]n and [Zn2(2)(OAc)4]n, the two outer nitrogen donors of the 4,2′:6′,4″-terpyridine ligands, bind to the axial sites of {Zn2(µ-OAc)4} units to generate coordination polymer chains which are π-stacked so that the V-shaped ligand domains are interleaved. When Mn(OAc)2·4H2O is treated with …
[Cu(bpy)(P^P)]+ containing light-emitting electrochemical cells: improving performance through simple substitution
2014
Light-emitting electrochemical cells (LECs) containing [Cu(POP)(N^N)][PF6] (POP = bis(2-diphenylphosphinophenyl)ether, N^N = 6-methyl- or 6,6′-dimethyl-2,2′-bipyridine) exhibit luminance and efficiency surpassing previous copper(i)-containing LECs.
Front Cover: CF3 Substitution of [Cu(P^P)(bpy)][PF6 ] Complexes: Effects on Photophysical Properties and Light-Emitting Electrochemical Cell Performa…
2018
The shiny side of copper: bringing copper(i) light-emitting electrochemical cells closer to application
2020
Heteroleptic [Cu(P^P)(N^N)][PF6] complexes, where N^N is 5,50-dimethyl-2,20-bipyridine (5,50-Me2bpy), 4,5,6-trimethyl-2,20-bipyridine (4,5,6-Me3bpy), 6-(tert-butyl)-2,20-bipyridine (6-tBubpy) and 2-ethyl-1,10- phenanthroline (2-Etphen) and P^P is either bis(2-(diphenylphosphino)phenyl)ether (POP, PIN [oxydi(2,1- phenylene)]bis(diphenylphosphane)) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos, PIN (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphane)) have been synthesized and their NMR spectroscopic, mass spectrometric, structural, electrochemical and photophysical properties were investigated. The single-crystal structures of [Cu(POP)(5,50-Me2bpy)][PF6], [Cu(xantphos)(5,…
Remote modification of bidentate phosphane ligands controlling the photonic properties in their complexes: Enhanced performance of [Cu(RN-xantphos)(N…
2020
A series of copper(I) complexes of the type [Cu(HN-xantphos)(N^N)][PF6] and [Cu(BnN-xantphos)(N^N)][PF6], in which N^N = bpy, Mebpy, and Me2bpy, HN-xantphos = 4,6-bis(diphenylphosphanyl)-10H-phenoxazine and BnNxantphos = 10-benzyl-4,6-bis(diphenylphosphanyl)-10H-phenoxazine is described. The single crystal structures of [Cu(HN-xantphos)(Mebpy)][PF6] and [Cu(BnN-xantphos)(Me2bpy)][PF6] confirm the presence of N^N and P^P chelating ligands with the copper(I) atoms in distorted coordination environments. Solution electrochemical and photophysical properties of the BnNxantphos- containing compounds (for which the highest-occupied molecular orbital is located on the phenoxazine moiety) are repor…
CCDC 2081388: Experimental Crystal Structure Determination
2021
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CCDC 1562407: Experimental Crystal Structure Determination
2018
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CCDC 1562410: Experimental Crystal Structure Determination
2018
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CCDC 2081386: Experimental Crystal Structure Determination
2021
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CCDC 1422375: Experimental Crystal Structure Determination
2016
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CCDC 974016: Experimental Crystal Structure Determination
2014
Related Article: Edwin C. Constable, Catherine E. Housecroft, Gabriel E. Schneider, Jennifer A. Zampese, Henk J. Bolink, Antonio Pertegás, Cristina Roldan-Carmona|2014|Dalton Trans.|43|4653|doi:10.1039/C3DT53477D
CCDC 974019: Experimental Crystal Structure Determination
2014
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CCDC 1515402: Experimental Crystal Structure Determination
2017
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CCDC 1584756: Experimental Crystal Structure Determination
2018
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CCDC 1486906: Experimental Crystal Structure Determination
2016
Related Article: Fabian Brunner, Laura Martínez-Sarti, Sarah Keller, Antonio Pertegás, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Catherine E. Housecroft|2016|Dalton Trans.|45|15180|doi:10.1039/C6DT02665F
CCDC 1584755: Experimental Crystal Structure Determination
2018
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CCDC 1422372: Experimental Crystal Structure Determination
2016
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CCDC 1486907: Experimental Crystal Structure Determination
2016
Related Article: Fabian Brunner, Laura Martínez-Sarti, Sarah Keller, Antonio Pertegás, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Catherine E. Housecroft|2016|Dalton Trans.|45|15180|doi:10.1039/C6DT02665F
CCDC 1486908: Experimental Crystal Structure Determination
2016
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CCDC 1844060: Experimental Crystal Structure Determination
2018
Related Article: Fabian Brunner, Azin Babaei, Antonio Pertegás, José M. Junquera-Hernández, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2019|Dalton Trans.|48|446|doi:10.1039/C8DT03827A
CCDC 1562409: Experimental Crystal Structure Determination
2018
Related Article: Murat Alkan-Zambada, Sarah Keller, Laura Martínez-Sarti, Alessandro Prescimone, José M. Junquera-Hernández, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2018|J.Mater.Chem.C|6|8460|doi:10.1039/C8TC02882F
CCDC 1978436: Experimental Crystal Structure Determination
2020
Related Article: Sarah Keller, Alessandro Prescimone, Maria-Grazia La Placa, José M. Junquera-Hernández, Henk J. Bolink, Edwin C. Constable, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2020|RSC Advances|10|22631|doi:10.1039/D0RA03824E
CCDC 972526: Experimental Crystal Structure Determination
2014
Related Article: Gabriel E. Schneider, Antonio Pertegás, Edwin C. Constable, Catherine E. Housecroft, Nik Hostettler, Collin D. Morris, Jennifer A. Zampese, Henk J. Bolink, José M. Junquera-Hernández, Enrique Ortí, Michele Sessolo|2014|J.Mater.Chem.C|2|7047|doi:10.1039/C4TC01171F
CCDC 1019228: Experimental Crystal Structure Determination
2015
Related Article: Andreas M. Bünzli, Edwin C. Constable, Catherine E. Housecroft, Alessandro Prescimone, Jennifer A. Zampese, Giulia Longo, Lidón Gil-Escrig, Antonio Pertegás, Enrique Ortí, Henk J. Bolink|2015|Chemical Science|6|2843|doi:10.1039/C4SC03942D
CCDC 1581155: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Fabian Brunner, José M. Junquera‐Hernández, Antonio Pertegás, Maria‐Grazia La‐Placa, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Enrique Ortí, Catherine E. Housecroft|2018|ChemPlusChem|83|217|doi:10.1002/cplu.201700501
CCDC 1535142: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Alessandro Prescimone, Henk Bolink, Michele Sessolo, Giulia Longo, Laura Martínez-Sarti, José M. Junquera-Hernández, Edwin C. Constable, Enrique Ortí, Catherine E. Housecroft|2018|Dalton Trans.|47|14263|doi:10.1039/C8DT01338A
CCDC 1844063: Experimental Crystal Structure Determination
2018
Related Article: Fabian Brunner, Azin Babaei, Antonio Pertegás, José M. Junquera-Hernández, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2019|Dalton Trans.|48|446|doi:10.1039/C8DT03827A
CCDC 2081394: Experimental Crystal Structure Determination
2021
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CCDC 1907394: Experimental Crystal Structure Determination
2020
Related Article: Nina Arnosti, Fabian Brunner, Isidora Susic, Sarah Keller, José M. Junquera‐Hernández, Alessandro Prescimone, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft, Edwin C. Constable|2020|Adv.Opt.Mater.|8|1901689|doi:10.1002/adom.201901689
CCDC 2081387: Experimental Crystal Structure Determination
2021
Related Article: Marco Meyer, Lorenzo Mardegan, Daniel Tordera, Alessandro Prescimone, Michele Sessolo, Henk J. Bolink, Edwin C. Constable, Catherine E. Housecroft|2021|Dalton Trans.|50|17920|doi:10.1039/D1DT03239A
CCDC 871500: Experimental Crystal Structure Determination
2013
Related Article: Edwin C. Constable, Markus Neuburger, Pirmin Rösel, Gabriel E. Schneider, Jennifer A. Zampese, Catherine E. Housecroft, Filippo Monti, Nicola Armaroli, Rubén D. Costa, and Enrique Ortí|2013|Inorg.Chem.|52|885|doi:10.1021/ic302026f
CCDC 1562458: Experimental Crystal Structure Determination
2018
Related Article: Murat Alkan-Zambada, Sarah Keller, Laura Martínez-Sarti, Alessandro Prescimone, José M. Junquera-Hernández, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2018|J.Mater.Chem.C|6|8460|doi:10.1039/C8TC02882F
CCDC 974020: Experimental Crystal Structure Determination
2014
Related Article: Edwin C. Constable, Catherine E. Housecroft, Gabriel E. Schneider, Jennifer A. Zampese, Henk J. Bolink, Antonio Pertegás, Cristina Roldan-Carmona|2014|Dalton Trans.|43|4653|doi:10.1039/C3DT53477D
CCDC 949190: Experimental Crystal Structure Determination
2013
Related Article: Andreas M. Bünzli, Henk J. Bolink, Edwin C. Constable, Catherine E. Housecroft, José M. Junquera-Hernández, Markus Neuburger, Enrique Ortí, Antonio Pertegás, Juan J. Serrano-Pérez, Daniel Tordera, Jennifer A. Zampese|2014|Dalton Trans.|43|738|doi:10.1039/C3DT52622D
CCDC 910854: Experimental Crystal Structure Determination
2013
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CCDC 1583875: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Alessandro Prescimone, Henk Bolink, Michele Sessolo, Giulia Longo, Laura Martínez-Sarti, José M. Junquera-Hernández, Edwin C. Constable, Enrique Ortí, Catherine E. Housecroft|2018|Dalton Trans.|47|14263|doi:10.1039/C8DT01338A
CCDC 959828: Experimental Crystal Structure Determination
2013
Related Article: Gabriel E. Schneider, Henk J. Bolink, Edwin C. Constable, Cathrin D. Ertl, Catherine E. Housecroft, Antonio Pertegàs, Jennifer A. Zampese, Andreas Kanitz, Florian Kessler, Sebastian B. Meier|2014|Dalton Trans.|43|1961|doi:10.1039/C3DT53229A
CCDC 1978440: Experimental Crystal Structure Determination
2020
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CCDC 1978441: Experimental Crystal Structure Determination
2020
Related Article: Sarah Keller, Alessandro Prescimone, Maria-Grazia La Placa, José M. Junquera-Hernández, Henk J. Bolink, Edwin C. Constable, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2020|RSC Advances|10|22631|doi:10.1039/D0RA03824E
CCDC 1584757: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Alessandro Prescimone, Henk Bolink, Michele Sessolo, Giulia Longo, Laura Martínez-Sarti, José M. Junquera-Hernández, Edwin C. Constable, Enrique Ortí, Catherine E. Housecroft|2018|Dalton Trans.|47|14263|doi:10.1039/C8DT01338A
CCDC 1562460: Experimental Crystal Structure Determination
2018
Related Article: Murat Alkan-Zambada, Sarah Keller, Laura Martínez-Sarti, Alessandro Prescimone, José M. Junquera-Hernández, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2018|J.Mater.Chem.C|6|8460|doi:10.1039/C8TC02882F
CCDC 1562411: Experimental Crystal Structure Determination
2018
Related Article: Murat Alkan-Zambada, Sarah Keller, Laura Martínez-Sarti, Alessandro Prescimone, José M. Junquera-Hernández, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2018|J.Mater.Chem.C|6|8460|doi:10.1039/C8TC02882F
CCDC 1429456: Experimental Crystal Structure Determination
2016
Related Article: Sarah Keller, Antonio Pertegás, Giulia Longo, Laura Martínez, Jesús Cerdá, José M. Junquera-Hernández, Alessandro Prescimone, Edwin C. Constable, Catherine E. Housecroft, Enrique Ortí, Henk J. Bolink|2016|J.Mater.Chem.C|4|3857|doi:10.1039/C5TC03725E
CCDC 1535141: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Alessandro Prescimone, Henk Bolink, Michele Sessolo, Giulia Longo, Laura Martínez-Sarti, José M. Junquera-Hernández, Edwin C. Constable, Enrique Ortí, Catherine E. Housecroft|2018|Dalton Trans.|47|14263|doi:10.1039/C8DT01338A
CCDC 871501: Experimental Crystal Structure Determination
2013
Related Article: Edwin C. Constable, Markus Neuburger, Pirmin Rösel, Gabriel E. Schneider, Jennifer A. Zampese, Catherine E. Housecroft, Filippo Monti, Nicola Armaroli, Rubén D. Costa, and Enrique Ortí|2013|Inorg.Chem.|52|885|doi:10.1021/ic302026f
CCDC 1486911: Experimental Crystal Structure Determination
2016
Related Article: Fabian Brunner, Laura Martínez-Sarti, Sarah Keller, Antonio Pertegás, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Catherine E. Housecroft|2016|Dalton Trans.|45|15180|doi:10.1039/C6DT02665F
CCDC 1019229: Experimental Crystal Structure Determination
2015
Related Article: Andreas M. Bünzli, Edwin C. Constable, Catherine E. Housecroft, Alessandro Prescimone, Jennifer A. Zampese, Giulia Longo, Lidón Gil-Escrig, Antonio Pertegás, Enrique Ortí, Henk J. Bolink|2015|Chemical Science|6|2843|doi:10.1039/C4SC03942D
CCDC 1584754: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Alessandro Prescimone, Henk Bolink, Michele Sessolo, Giulia Longo, Laura Martínez-Sarti, José M. Junquera-Hernández, Edwin C. Constable, Enrique Ortí, Catherine E. Housecroft|2018|Dalton Trans.|47|14263|doi:10.1039/C8DT01338A
CCDC 1562408: Experimental Crystal Structure Determination
2018
Related Article: Murat Alkan-Zambada, Sarah Keller, Laura Martínez-Sarti, Alessandro Prescimone, José M. Junquera-Hernández, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2018|J.Mater.Chem.C|6|8460|doi:10.1039/C8TC02882F
CCDC 974892: Experimental Crystal Structure Determination
2016
Related Article: Cathrin D. Ertl, Henk J. Bolink, Catherine E. Housecroft, Edwin C. Constable, Enrique Ortí, José M. Junquera-Hernández, Markus Neuburger, Nail M. Shavaleev, Mohammad Khaja Nazeeruddin and David Vonlanthen|2016|Eur.J.Org.Chem.|2016|2037|doi:10.1002/ejoc.201600247
CCDC 1515401: Experimental Crystal Structure Determination
2017
Related Article: Cristina Momblona, Cathrin D. Ertl, Antonio Pertegás, José M. Junquera-Hernández, Maria-Grazia La-Placa, Alessandro Prescimone, Enrique Ortí, Catherine E. Housecroft, Edwin C. Constable, and Henk J. Bolink|2017|J.Am.Chem.Soc.|139|3237|doi:10.1021/jacs.6b13311
CCDC 1581154: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Fabian Brunner, José M. Junquera‐Hernández, Antonio Pertegás, Maria‐Grazia La‐Placa, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Enrique Ortí, Catherine E. Housecroft|2018|ChemPlusChem|83|217|doi:10.1002/cplu.201700501
CCDC 1422374: Experimental Crystal Structure Determination
2016
Related Article: Sarah Keller, Antonio Pertegás, Giulia Longo, Laura Martínez, Jesús Cerdá, José M. Junquera-Hernández, Alessandro Prescimone, Edwin C. Constable, Catherine E. Housecroft, Enrique Ortí, Henk J. Bolink|2016|J.Mater.Chem.C|4|3857|doi:10.1039/C5TC03725E
CCDC 2081391: Experimental Crystal Structure Determination
2021
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CCDC 1421913: Experimental Crystal Structure Determination
2016
Related Article: Cathrin D. Ertl, Lidón Gil-Escrig, Jesús Cerdá, Antonio Pertegás, Henk J. Bolink, José M. Junquera-Hernández, Alessandro Prescimone, Markus Neuburger, Edwin C. Constable, Enrique Ortí, Catherine E. Housecroft|2016|Dalton Trans.|45|11668|doi:10.1039/C6DT01325B
CCDC 1581156: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Fabian Brunner, José M. Junquera‐Hernández, Antonio Pertegás, Maria‐Grazia La‐Placa, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Enrique Ortí, Catherine E. Housecroft|2018|ChemPlusChem|83|217|doi:10.1002/cplu.201700501
CCDC 2081389: Experimental Crystal Structure Determination
2021
Related Article: Marco Meyer, Lorenzo Mardegan, Daniel Tordera, Alessandro Prescimone, Michele Sessolo, Henk J. Bolink, Edwin C. Constable, Catherine E. Housecroft|2021|Dalton Trans.|50|17920|doi:10.1039/D1DT03239A
CCDC 1562448: Experimental Crystal Structure Determination
2018
Related Article: Murat Alkan-Zambada, Sarah Keller, Laura Martínez-Sarti, Alessandro Prescimone, José M. Junquera-Hernández, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2018|J.Mater.Chem.C|6|8460|doi:10.1039/C8TC02882F
CCDC 1421914: Experimental Crystal Structure Determination
2016
Related Article: Cathrin D. Ertl, Lidón Gil-Escrig, Jesús Cerdá, Antonio Pertegás, Henk J. Bolink, José M. Junquera-Hernández, Alessandro Prescimone, Markus Neuburger, Edwin C. Constable, Enrique Ortí, Catherine E. Housecroft|2016|Dalton Trans.|45|11668|doi:10.1039/C6DT01325B
CCDC 949192: Experimental Crystal Structure Determination
2013
Related Article: Andreas M. Bünzli, Henk J. Bolink, Edwin C. Constable, Catherine E. Housecroft, José M. Junquera-Hernández, Markus Neuburger, Enrique Ortí, Antonio Pertegás, Juan J. Serrano-Pérez, Daniel Tordera, Jennifer A. Zampese|2014|Dalton Trans.|43|738|doi:10.1039/C3DT52622D
CCDC 2081393: Experimental Crystal Structure Determination
2021
Related Article: Marco Meyer, Lorenzo Mardegan, Daniel Tordera, Alessandro Prescimone, Michele Sessolo, Henk J. Bolink, Edwin C. Constable, Catherine E. Housecroft|2021|Dalton Trans.|50|17920|doi:10.1039/D1DT03239A
CCDC 1562457: Experimental Crystal Structure Determination
2018
Related Article: Murat Alkan-Zambada, Sarah Keller, Laura Martínez-Sarti, Alessandro Prescimone, José M. Junquera-Hernández, Edwin C. Constable, Henk J. Bolink, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2018|J.Mater.Chem.C|6|8460|doi:10.1039/C8TC02882F
CCDC 1019226: Experimental Crystal Structure Determination
2015
Related Article: Andreas M. Bünzli, Edwin C. Constable, Catherine E. Housecroft, Alessandro Prescimone, Jennifer A. Zampese, Giulia Longo, Lidón Gil-Escrig, Antonio Pertegás, Enrique Ortí, Henk J. Bolink|2015|Chemical Science|6|2843|doi:10.1039/C4SC03942D
CCDC 1581157: Experimental Crystal Structure Determination
2018
Related Article: Sarah Keller, Fabian Brunner, José M. Junquera‐Hernández, Antonio Pertegás, Maria‐Grazia La‐Placa, Alessandro Prescimone, Edwin C. Constable, Henk J. Bolink, Enrique Ortí, Catherine E. Housecroft|2018|ChemPlusChem|83|217|doi:10.1002/cplu.201700501
CCDC 974017: Experimental Crystal Structure Determination
2014
Related Article: Edwin C. Constable, Catherine E. Housecroft, Gabriel E. Schneider, Jennifer A. Zampese, Henk J. Bolink, Antonio Pertegás, Cristina Roldan-Carmona|2014|Dalton Trans.|43|4653|doi:10.1039/C3DT53477D
CCDC 974022: Experimental Crystal Structure Determination
2014
Related Article: Edwin C. Constable, Catherine E. Housecroft, Gabriel E. Schneider, Jennifer A. Zampese, Henk J. Bolink, Antonio Pertegás, Cristina Roldan-Carmona|2014|Dalton Trans.|43|4653|doi:10.1039/C3DT53477D
CCDC 974021: Experimental Crystal Structure Determination
2014
Related Article: Edwin C. Constable, Catherine E. Housecroft, Gabriel E. Schneider, Jennifer A. Zampese, Henk J. Bolink, Antonio Pertegás, Cristina Roldan-Carmona|2014|Dalton Trans.|43|4653|doi:10.1039/C3DT53477D
CCDC 1009455: Experimental Crystal Structure Determination
2014
Related Article: Sarah Keller, Edwin C. Constable, Catherine E. Housecroft, Markus Neuburger, Alessandro Prescimone, Giulia Longo, Antonio Pertegás, Michele Sessolo, Henk J. Bolink|2014|Dalton Trans.|43|16593|doi:10.1039/C4DT02847C
CCDC 2081390: Experimental Crystal Structure Determination
2021
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CCDC 1055780: Experimental Crystal Structure Determination
2015
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CCDC 1844062: Experimental Crystal Structure Determination
2018
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CCDC 1562453: Experimental Crystal Structure Determination
2018
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CCDC 974023: Experimental Crystal Structure Determination
2014
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CCDC 1486909: Experimental Crystal Structure Determination
2016
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CCDC 1421915: Experimental Crystal Structure Determination
2016
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CCDC 949191: Experimental Crystal Structure Determination
2013
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CCDC 1978437: Experimental Crystal Structure Determination
2020
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CCDC 971737: Experimental Crystal Structure Determination
2013
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CCDC 974018: Experimental Crystal Structure Determination
2014
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CCDC 1844061: Experimental Crystal Structure Determination
2018
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CCDC 996509: Experimental Crystal Structure Determination
2014
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CCDC 1581158: Experimental Crystal Structure Determination
2018
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CCDC 1486910: Experimental Crystal Structure Determination
2016
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CCDC 1562412: Experimental Crystal Structure Determination
2018
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CCDC 1535144: Experimental Crystal Structure Determination
2018
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CCDC 1860879: Experimental Crystal Structure Determination
2018
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CCDC 1978438: Experimental Crystal Structure Determination
2020
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CCDC 1581159: Experimental Crystal Structure Determination
2018
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CCDC 1422373: Experimental Crystal Structure Determination
2016
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CCDC 1584752: Experimental Crystal Structure Determination
2018
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CCDC 1062206: Experimental Crystal Structure Determination
2017
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CCDC 1562449: Experimental Crystal Structure Determination
2018
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CCDC 871502: Experimental Crystal Structure Determination
2013
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CCDC 2081392: Experimental Crystal Structure Determination
2021
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CCDC 993287: Experimental Crystal Structure Determination
2016
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CCDC 1907395: Experimental Crystal Structure Determination
2020
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CCDC 1978442: Experimental Crystal Structure Determination
2020
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CCDC 974893: Experimental Crystal Structure Determination
2016
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CCDC 1584753: Experimental Crystal Structure Determination
2018
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CCDC 1435492: Experimental Crystal Structure Determination
2016
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CCDC 1535143: Experimental Crystal Structure Determination
2018
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CCDC 1978439: Experimental Crystal Structure Determination
2020
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CCDC 1019227: Experimental Crystal Structure Determination
2015
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