0000000001299702
AUTHOR
Robin H. A. Ras
showing 70 related works from this author
N-Alkyl Ammonium Resorcinarene Salts as High-Affinity Tetravalent Chloride Receptors.
2016
N-Alkyl ammonium resorcinarene salts (NARYs, Y=triflate, picrate, nitrate, trifluoroacetates and NARBr) as tetravalent receptors, are shown to have a strong affinity for chlorides. The high affinity for chlorides was confirmed from a multitude of exchange experiments in solution (NMR and UV/Vis), gas phase (mass spectrometry), and solid-state (X-ray crystallography). A new tetra-iodide resorcinarene salt (NARI) was isolated and fully characterized from exchange experiments in the solid-state. Competition experiments with a known monovalent bis-urea receptor (5) with strong affinity for chloride, reveals these receptors to have a much higher affinity for the first two chlorides, a similar af…
Guest-Induced Folding of the N-Benzyl Substituents in an Ammonium Resorcinarene Chloride and the Formation of a Halogen-Bonded Dimer of Capsules
2016
In methanol, N-benzyl ammonium resorcinarene chloride (Bn-NARCl) crystallizes as a solvate with the benzyl groups oriented in an open flower-like manner parallel to the cation–anion seam. 1,4-Dioxane as guest triggers a “semi-closed” single-molecule capsule with two benzyl “arms” enclosing the guest. The introduction of halogen bond (XB) donor 1,4-diiodoperfluorobutane (1,4-DIOFB) additionally folds the remaining two benzyl arms thus resulting in a fully closed capsule. Two 1,4-DIOFB molecules bridge two such Bn-NARCl capsules, forming a 2:2:2 XB held dimeric assembly of single-molecule capsules. The peculiar behavior was not observed in the bromide analog under similar experimental conditi…
High-affinity and selective detection of pyrophosphate in water by a resorcinarene salt receptor
2017
N-Alkyl ammonium resorcinarenes selectively bind pyrophosphate in pure water with an exceptionally high binding constant of up to 1.60 × 107 M–1, three orders of magnitude higher than ATP.
Core‐Selective Silver‐Doping of Gold Nanoclusters by Surface‐Bound Sulphates on Colloidal Templates: From Synthetic Mechanism to Relaxation Dynamics
2022
Funding Information: This work was carried out under the ERC Advanced grant (DRIVEN, ERC‐2016‐AdG‐742829), Academy of Finland's Centre of Excellence in Life‐Inspired Hybrid Materials (LIBER, 346108), Academy of Finland (No. 321443, 328942, 308647, and 318891) and Photonic Research and Innovation (PREIN) as well as FinnCERES flagships. L.F. and X.C. thanks for support from CSC (IT Center for Science, Finland) for providing computation resources. The authors acknowledge the provision of facilities and technical support by Aalto University OtaNano – Nanomicroscopy Center (Aalto‐NMC). | openaire: EC/H2020/742829/EU//DRIVEN Ultra-small luminescent gold nanoclusters (AuNCs) have gained substantia…
Host-Guest Complexes of C-Ethyl-2-methylresorcinarene and Aromatic N,N′-Dioxides
2017
The C‐ethyl‐2‐methylresorcinarene (1) forms 1:1 in‐cavity complexes with aromatic N,N′‐dioxides, only if each of the aromatic rings has an N−O group. The structurally different C‐shaped 2,2′‐bipyridine N,N′‐dioxide (2,2′‐BiPyNO) and the linear rod‐shaped 4,4′‐bipyridine N,N′‐dioxide (4,4′‐BiPyNO) both form 1:1 in‐cavity complexes with the host resorcinarene in C4v crown and C2v conformations, respectively. In the solid state, the host–guest interactions between the 1,3‐bis(4‐pyridyl)propane N,N′‐dioxide (BiPyPNO) and the host 1 stabilize the unfavorable anti‐gauche conformation. Contrary to the N,N′‐dioxide guests, the mono‐N‐oxide guest, 4‐phenylpyridine N‐oxide (4PhPyNO), does not form an…
Gold Au(I)6 Clusters with Ligand-Derived Atomic Steric Locking: Multifunctional Optoelectrical Properties and Quantum Coherence
2023
Funding Information: This work was supported by the ERC Advanced grant (DRIVEN, ERC‐2016‐AdG‐742829), the ERC grant (834742), the EU H2020‐MSCA‐RISE‐872049 (IPN‐Bio), the Academy of Finland's Centre of Excellence in Molecular Engineering of Biosynthetic Hybrid Materials Research (HYBER, 2014–2019), and Life‐Inspired Hybrid Materials (LIBER, 346108), Academy of Finland project fundings (No. 352900, 314810, 333982, 336144, 352780, 352930 and 353364), FinnCERES and Photonics Research and Innovation (PREIN) flagship programs. The authors acknowledge the provision of facilities and technical support by Aalto University OtaNano – Nanomicroscopy Center (Aalto‐NMC). | openaire: EC/H2020/834742/EU//…
Recognition of Viologen Derivatives in Water by N-Alkyl Ammonium Resorcinarene Chlorides
2017
Three water-soluble N-alkyl ammonium resorcinarene chlorides decorated with terminal hydroxyl groups at the lower rims were synthesized and characterized. The receptors were decorated at the upper rim with either terminal hydroxyl, rigid cyclohexyl, or flexible benzyl groups. The binding affinities of these receptors toward three viologen derivatives, two of which possess an acetylmethyl group attached to one of the pyridine nitrogens, in water were investigated via 1H NMR spectroscopy, fluorescence spectroscopy, and isothermal titration calorimetry (ITC). ITC quantification of the binding process gave association constants of up to 103 M–1. Analyses reveal a spontaneous binding process whi…
Halogen-bonded solvates of tetrahaloethynyl cavitands
2017
The formation and structures of halogen-bonded solvates of three different tetrahaloethynyl cavitands with acetone, chloroform, acetonitrile, DMF and DMSO were prepared and investigated. The inclusion and host–guest behaviour of the resorcinarene cavitands was found to be highly dependent on the flexibility of the ethylene-bridging unit.
Bamboo-like Chained Cavities and Other Halogen-Bonded Complexes from Tetrahaloethynyl Cavitands with Simple Ditopic Halogen Bond Acceptors
2018
Halogen bonding provides a useful complement to hydrogen bonding and metal-coordination as a tool for organizing supramolecular systems. Resorcinarenes, tetrameric bowl-shaped cavitands, have been previously shown to function as efficient scaffolds for generating dimeric capsules in both solution and solid-phase, and complicated one-, two-, and three-dimensional frameworks in the solid phase. Tetrahaloethynyl resorcinarenes (bromide and iodide) position the halogen atoms in a very promising “crown-like” orientation for acting as organizing halogen-bond donors to help build capsules and higher-order networks. Symmetric divalent halogen bond acceptors including bipyridines, 1,4-dioxane, and 1…
2-Methylresorcinarene: a very high packing coefficient in a mono-anion based dimeric capsule and the X-ray crystal structure of the tetra-anion
2016
Mono- and tetra-deprotonated 2-methylresorcinarene anions (1 and 2) as their trans-1,4-diammoniumcyclohexane (TDAC)2+ inclusion complexes are reported. The mono-anion forms a fully closed dimeric capsule [1·H2O·MeOH]22− with a cavity volume of 165 Å3 and (TDAC)2+ as the guest with an extremely high packing coefficient, PC = 84.2%, while the tetra-anion forms a close-packed structure with two structurally isomeric tetra-anions 2a and 2b with a 50 : 50 ratio in the crystal lattice. peerReviewed
N-Alkyl ammonium resorcinarene polyiodides
2016
Four N-alkyl ammonium resorcinarene halides incorporating polyiodides were obtained and structurally analyzed by single crystal X-ray crystallography. The unexpected formation of triiodides and pentaiodide anions in these structures was assumed to be the result of the heterolytic dissociation of molecular iodine (I2) in the presence of electron donors in the N-alkyl ammonium resorcinarene halide system, from which I− further binds one or two I2 molecules resulting in I3− or I5− species, respectively.
Host-guest complexes of C-propyl-2-bromoresorcinarene with aromatic N-oxides*
2018
The host-guest complexes of C-propyl-2-bromoresorcinarene with pyridine N-oxide, 3-methylpyridine N-oxide, quinoline N-oxide and isoquinoline N-oxide are studied using single crystal X-ray crystallography and 1H NMR spectroscopy. The C-propyl-2-bromoresorcinarene forms endo-complexes with the aromatic N-oxides in the solid-state when crystallised from either methanol or acetone. In solution, the endo-complexes were observed only in methanol-d4. In DMSO the solvent itself is a good guest, and crystallisation provides only solvate endo-complexes. The C-propyl-2-bromoresorcinarene shows remarkable flexibility when crystallised from either methanol or acetone, and packs into one-dimensional sel…
Endo-/exo- and halogen-bonded complexes of conformationally rigid C-ethyl-2-bromoresorcinarene and aromatic N-oxides
2017
The host-guest complexes of conformationally rigid C-ethyl-2-bromoresorcinarene with aromatic N-oxides were studied using single crystal X-ray crystallography. Unlike that of the conformationally more flexible C-ethyl-2-methylresorcinarene, the C-ethyl-2-bromoresorcinarene cavity forms endo-complexes only with the small pyridine-N-oxides, such as pyridine N-oxide, 2-methyl-, 3-methyl- and 4-methylpyrdine N-oxide, and quinoline N-oxide. The larger 2,4,6-trimethylpyridine, 4-phenylpyridine and isoquinoline N-oxide, and 4,4-bipyridine N,N′-dioxide and 1,3-bis(4-pyridyl)propane N,N′-dioxide do not fit into the host cavity. Instead endo-acetone complexes are formed. Remarkably, differing from th…
Review article: recommended reading list of early publications on atomic layer deposition - outcome of the "virtual Project on the History of ALD"
2017
Atomic layer deposition (ALD), a gas-phase thin film deposition technique based on repeated, self-terminating gas-solid reactions, has become the method of choice in semiconductor manufacturing and many other technological areas for depositing thin conformal inorganic material layers for various applications. ALD has been discovered and developed independently, at least twice, under different names: atomic layer epitaxy (ALE) and molecular layering. ALE, dating back to 1974 in Finland, has been commonly known as the origin of ALD, while work done since the 1960s in the Soviet Union under the name "molecular layering" (and sometimes other names) has remained much less known. The virtual proj…
N-Alkyl Ammonium Resorcinarene Chloride Receptors for Guest Binding in Aqueous Environment
2016
Host systems with guest binding ability in water and/or biological fluids are a current challenge in supramolecular host–guest chemistry. Here we present the first syntheses of water-soluble N-ethanol ammonium resorcinarene chlorides (NARCls) with terminal hydroxyl groups at the upper rim. The NARCls possess deep cavities and are shown to bind a variety of guest molecules such as linear and cyclic alkanes, linear halogenated alkanes, and aromatic fluorophores (naphthalene, p-(phenylazo)phenol) in water through hydrophobic interactions, as well as 1,4-dioxane (a water soluble guest) via hydrogen bonds. The receptors are monomeric in aqueous media and form 1:1 host–guest complexes with bindin…
The Recognition of Viologen Derivatives in Water by N-Alkyl Ammonium Resorcinarene Chlorides
2017
Three water-soluble N-alkyl ammonium resorcinarene chlorides decorated with terminal hydroxyl groups at the lower rims were synthesized and characterized. The receptors were decorated at the upper rim with either terminal hydroxyl, rigid cyclohexyl, or flexible benzyl groups. The binding affinities of these receptors toward three viologen derivatives, two of which possess an acetylmethyl group attached to one of the pyridine nitrogens, in water were investigated via 1H NMR spectroscopy, fluorescence spectroscopy, and isothermal titration calorimetry (ITC). ITC quantification of the binding process gave association constants of up to 103 M-1. Analyses reveal a spontaneous binding process whi…
Host-guest complexes of C-propyl-2-bromoresorcinarene with aromatic N-oxides*
2017
The host-guest complexes of C-propyl-2-bromoresorcinarene with pyridine N-oxide, 3-methylpyridine N-oxide, quinoline N-oxide and isoquinoline N-oxide are studied using single crystal X-ray crystallography and 1H NMR spectroscopy. The C-propyl-2-bromoresorcinarene forms endo-complexes with the aromatic N-oxides in the solid-state when crystallised from either methanol or acetone. In solution, the endo-complexes were observed only in methanol-d4. In DMSO the solvent itself is a good guest, and crystallisation provides only solvate endo-complexes. The C-propyl-2-bromoresorcinarene shows remarkable flexibility when crystallised from either methanol or acetone, and packs into one-dimensional sel…
CCDC 1481997: Experimental Crystal Structure Determination
2016
Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|CrystEngComm|18|5724|doi:10.1039/C6CE01229A
CCDC 1551407: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1551402: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1525503: Experimental Crystal Structure Determination
2017
Related Article: Ngong Kodiah Beyeh, Hyun Hwa Jo, Igor Kolesnichenko, Fangfang Pan, Elina Kalenius, Eric V. Anslyn, Robin H. A. Ras, Kari Rissanen|2017|J.Org.Chem.|82|5198|doi:10.1021/acs.joc.7b00449
CCDC 1556027: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 1583123: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1488064: Experimental Crystal Structure Determination
2016
Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|Cryst.Growth Des.|16|6729|doi:10.1021/acs.cgd.6b01454
CCDC 1429823: Experimental Crystal Structure Determination
2016
Related Article: N. Kodiah Beyeh, Fangfang Pan, Sandip Bhowmik, Toni Mäkelä, Robin H. A. Ras, Kari Rissanen|2016|Chem.-Eur.J.|22|1355|doi:10.1002/chem.201504514
CCDC 1429824: Experimental Crystal Structure Determination
2016
Related Article: N. Kodiah Beyeh, Fangfang Pan, Sandip Bhowmik, Toni Mäkelä, Robin H. A. Ras, Kari Rissanen|2016|Chem.-Eur.J.|22|1355|doi:10.1002/chem.201504514
CCDC 1488067: Experimental Crystal Structure Determination
2016
Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|Cryst.Growth Des.|16|6729|doi:10.1021/acs.cgd.6b01454
CCDC 1429822: Experimental Crystal Structure Determination
2016
Related Article: N. Kodiah Beyeh, Fangfang Pan, Sandip Bhowmik, Toni Mäkelä, Robin H. A. Ras, Kari Rissanen|2016|Chem.-Eur.J.|22|1355|doi:10.1002/chem.201504514
CCDC 1551412: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1583131: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1452468: Experimental Crystal Structure Determination
2016
Related Article: Ngong Kodiah Beyeh, Fangfang Pan, Robin H. A. Ras|2016|Asian J.Org.Chem|5|1027|doi:10.1002/ajoc.201600187
CCDC 1556030: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 1481998: Experimental Crystal Structure Determination
2016
Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|CrystEngComm|18|5724|doi:10.1039/C6CE01229A
CCDC 1583125: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1556033: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 1583130: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1551404: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1583128: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1574172: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, John F. Trant, Robin H. A. Ras, Kari Rissanen|2018|Cryst.Growth Des.|18|513|doi:10.1021/acs.cgd.7b01517
CCDC 1481996: Experimental Crystal Structure Determination
2016
Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|CrystEngComm|18|5724|doi:10.1039/C6CE01229A
CCDC 1488066: Experimental Crystal Structure Determination
2016
Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|Cryst.Growth Des.|16|6729|doi:10.1021/acs.cgd.6b01454
CCDC 1452743: Experimental Crystal Structure Determination
2016
Related Article: Ngong Kodiah Beyeh, Fangfang Pan, Robin H. A. Ras|2016|Asian J.Org.Chem|5|1027|doi:10.1002/ajoc.201600187
CCDC 1551411: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1574174: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, John F. Trant, Robin H. A. Ras, Kari Rissanen|2018|Cryst.Growth Des.|18|513|doi:10.1021/acs.cgd.7b01517
CCDC 1556029: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 1551410: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1488065: Experimental Crystal Structure Determination
2016
Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|Cryst.Growth Des.|16|6729|doi:10.1021/acs.cgd.6b01454
CCDC 1583127: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1525501: Experimental Crystal Structure Determination
2017
Related Article: Ngong Kodiah Beyeh, Hyun Hwa Jo, Igor Kolesnichenko, Fangfang Pan, Elina Kalenius, Eric V. Anslyn, Robin H. A. Ras, Kari Rissanen|2017|J.Org.Chem.|82|5198|doi:10.1021/acs.joc.7b00449
CCDC 1551408: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1556032: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 1551406: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1551403: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1574171: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, John F. Trant, Robin H. A. Ras, Kari Rissanen|2018|Cryst.Growth Des.|18|513|doi:10.1021/acs.cgd.7b01517
CCDC 1529901: Experimental Crystal Structure Determination
2021
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2017|ChemistryOpen|6|417|doi:10.1002/open.201700026
CCDC 1529902: Experimental Crystal Structure Determination
2021
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2017|ChemistryOpen|6|417|doi:10.1002/open.201700026
CCDC 1583124: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1525502: Experimental Crystal Structure Determination
2017
Related Article: Ngong Kodiah Beyeh, Hyun Hwa Jo, Igor Kolesnichenko, Fangfang Pan, Elina Kalenius, Eric V. Anslyn, Robin H. A. Ras, Kari Rissanen|2017|J.Org.Chem.|82|5198|doi:10.1021/acs.joc.7b00449
CCDC 1556028: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 1551405: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1583126: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1583122: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1529904: Experimental Crystal Structure Determination
2021
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2017|ChemistryOpen|6|417|doi:10.1002/open.201700026
CCDC 1429821: Experimental Crystal Structure Determination
2016
Related Article: N. Kodiah Beyeh, Fangfang Pan, Sandip Bhowmik, Toni Mäkelä, Robin H. A. Ras, Kari Rissanen|2016|Chem.-Eur.J.|22|1355|doi:10.1002/chem.201504514
CCDC 1583129: Experimental Crystal Structure Determination
2018
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Pia Jurcek, Lotta Turunen, John F. Trant, Robin H. A. Ras and Kari Rissanen|2017|Supramol.Catal.|30|445|doi:10.1080/10610278.2017.1414217
CCDC 1551401: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1481999: Experimental Crystal Structure Determination
2016
Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|CrystEngComm|18|5724|doi:10.1039/C6CE01229A
CCDC 1556031: Experimental Crystal Structure Determination
2017
Related Article: Lotta Turunen, Fangfang Pan, Ngong Kodiah Beyeh, Mario Cetina, John F. Trant, Robin H. A. Ras, Kari Rissanen|2017|CrystEngComm|19|5223|doi:10.1039/C7CE01118K
CCDC 1551409: Experimental Crystal Structure Determination
2017
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E
CCDC 1529903: Experimental Crystal Structure Determination
2021
Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2017|ChemistryOpen|6|417|doi:10.1002/open.201700026