Cooperative supramolecular polymerization and amplification of chirality in C3-symmetrical OPE-based trisamides.

Sergeants-and-soldiers experiments demonstrate the amplification of chirality that transforms the racemic mixture of helical columns formed from OPE-based trisamides into enantiomerically enriched helical structures (see scheme).The cooperative supramolecular polymerization of the trisamides is investigated by theoretical calculations and temperature-dependent UV/Vis and CD experiments. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Frontispiece: Hierarchy of Asymmetry at Work: Chain-Dependent Helix-to-Helix Interactions in Supramolecular Polymers

Dumbbell-Shaped Dinuclear Iridium Complexes and Their Application to Light-Emitting Electrochemical Cells

A novel family of dumbbell- shaped dinuclear complexes in which an oligophenyleneethynylene spacer is linked to two heteroleptic iridiumA complexes is presented. The synthesis, as well as the electrochemical and pho- tophysical characterization of the new complexes, is reported. The experimen- tal results are interpreted with the help of density functional theory calcula- tions. From these studies we conclude that the lowest triplet excited state cor- responds to a 3 p-p* state located on the conjugated spacer. The presence of this state below the 3 MLCT/ 3 LLCT emitting states of the end-capping Ir III complexes explains the low quantum yields observed for the dinuclear com- plexes (one or…

Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness.

The cooperative supramolecular polymerization of 1 and 2 yields P- or M-type helical aggregates depending on the absolute configuration (S or R) of the stereogenic centres attached to the side chains. The connectivity of the amide group does not affect the handedness of the helical aggregates, but determines a larger cooperativity for retroamides 1.

Sermon en la octava que en esta Corte se consagrò a la gloria de los veinte y tres Martires del Iapon, Descalços de la Orden de San Francisco, que canonizó ... Vrbano VIII

Grav. a la port Sign.: A-D4 Postil·les marginals

Acene-type donors bearing one 1,3-dithiole ring

Abstract A series of acene-type donors bearing only one 1,3-dithiole ring have been synthesized by following a Wittig-Horner reaction from 7 H -benz[ d,e ]anthracen-7-one and several phosphonate esters. The excellent donor properties have been studied using both experimental techniques and quantum-chemical calculations and reveal that the extraction of the first electron in the oxidation process occurs from the dithiole ring (0.42 e) and the acene unit (0.58 e).

Synergy of Axial and Point Chirality to Construct Helical N -Heterotriangulene-Based Supramolecular Polymers

Supramolecular polymerization of electronically complementary linear motifs: anti-cooperativity by attenuated growth†

Anti-cooperative supramolecular polymerization by attenuated growth exhibited by self-assembling units of two electron-donor benzo[1,2-b:4,5-b′]dithiophene (BDT) derivatives (compounds 1a and 1b) and the electron-acceptor 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) (compound 2) is reported. Despite the apparent cooperative mechanism of 1 and 2, AFM imaging and SAXS measurements reveal the formation of small aggregates that suggest the operation of an anti-cooperative mechanism strongly conditioned by an attenuated growth. In this mechanism, the formation of the nuclei is favoured over the subsequent addition of monomeric units to the aggregate, which finally results in short aggrega…

Concave Tetrathiafulvalene-Type Donors as Supramolecular Partners for Fullerenes

The cap fits! A new class of concave π-extended tetrathiafulvalene (TTF) derivatives, truxene-TTFs, were prepared and characterized, and their self-assembly with fullerenes was investigated (see picture). Truxene-TTFs represent the first example of TTF-related electron donors that serve, without chemical modification, as monotopic receptors for fullerenes in solution. (Chemical Equation Presented). © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.

Weighting non-covalent forces in the molecular recognition of C60. Relevance of concave–convex complementarity

The relative contributions of several weak intermolecular forces to the overall stability of the complexes formed between structurally related receptors and [60]fullerene are compared, revealing a discernible contribution from concave–convex complementarity. Viruela Martin, Pedro Manuel, Pedro.M.Viruela@uv.es ; Viruela Martin, Rafael, Rafael.Viruela@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es

Segunda parte del Nobiliario genealogico de los reyes i titulos de España

Inclou indexs I. [16], 400 [i.e.606], [8] p. Sign.: ¶8, A-H8, I10, K-Cc8, Dd9, Ee-Nn8, Oo10, Pp2, ¶4. Errors de pag.: 135-138 foliats, de la p. 428 passa a la 427, de la 596 a la 397 II. Segunda parte del Nobiliario genealogico de los reyes i titulos de España ... / compuesto por Alonso Lopez de Haro ... . En Madrid : por la viuda de Fernando Correa de Montenegro, 1622. 532, [8] p. Sign.: a-kk8, ll6. - Colofó en p. 53. - Els grav. de les p. 348 i 355 calc Els grav. xil., escuts d'armes i arbres genealògics Escut xil. de Felip IV, a qui es dedica l'obra, a les port Caplletres i altres ornaments tip Text a dues col., amb postil·les marginals Reclams

On the handedness of helical aggregates of C3 tricarboxamides: a multichiroptical characterization

A complete chiroptical characterization of the supramolecular polymers formed by tricarboxamides (S)-1 and (R)-1 is performed using ECD, VCD and CPL dichroic techniques. The helical aggregates show an intense CPL signal and their absolute P- or M-configuration is assigned with the help of theoretical calculations.

Donor-π-Acceptor Species Derived from Functionalised 1,3-Dithiol-2-ylidene Anthracene Donor Units Exhibiting Photoinduced Electron Transfer Properties: Spectroscopic, Electrochemical, X-Ray Crystallographic and Theoretical Studies

Steric interactions between the anthraquinoid core and the 1,3-dithiole and dicyanomethylene groups play a key role in determining the physical properties of system 1. The intramolecular charge transfer properties of this donor–π-acceptor species have been explored and cyclic voltammetric data, X-ray crystal structures and ab initio calculations are also reported.

Innenrücktitelbild: N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates (Angew. Chem. 40/2020)

Breue relacion de la milagrosa y celestial imagen de Santo Domingo, Patriarcha de la Orden de Predicadores, trayda del Cielo por mano de la Virgen ... Al conuento de Santo Domingo de Soriano, en el Reyno de Napoles, cuya copia esta en el Colegio de Santo Thomas de Madrid ... : Sacado todo del libro que en toscano hizo imprimir el dicho Conuento

Text a dues col Sign.: [ ]2

A bis(triazole)benzamide receptor for the complexation of halide anions and neutral carboxylic acid guests. Guest-controlled topicity and self-assembly

Bis(triazole)benzamide 1 has been readily synthesized by means of Cu-catalyzed 1,3-dipolar cycloaddition and its ability to bind halide anions and neutral gallic acid derivative 12GA has been theoretically and experimentally investigated. The cavity defined by the N-H amide group and the vicinal aromatic hydrogens is suitable to form H-bonding arrays with halide guests. The stability of complexes 1·Cl- and 1·Br- is very similar, as DFT calculations predict and 1H NMR titration experiments confirm. The zigzag "anti" conformation of the molecule generates two regions with complementary positive and negative potentials that favor the statistical complexation of two molecules of the neutral car…

Hierarchy of Asymmetry at Work: Chain-Dependent Helix-to-Helix Interactions in Supramolecular Polymers.

A detailed investigation of the hierarchy of asymmetry operating in the self-assembly of achiral (1) and chiral ((S)-2 and (R)-3) 1,3,5-triphenylbenzenetricarboxamides (TPBAs) is reported. The aggregation of these TPBAs is conditioned by the point chirality at the peripheral side chains for (S)-2 and (R)-3. An efficient helix-to-helix interaction that goes further in the organization of fibrillar bundles is experimentally detected and theoretically supported only for the achiral TPBA 1. The effective interdigitation of the achiral aliphatic side chains produces a social self-sorting to form preferentially heterochiral macromolecular aggregates.

Mesocrystalline Cr and Sb-codoped anatase visible-light-driven photocatalyst

Abstract We report on the synthesis, characterization and visible-light-driven photocatalytic activity of mesocrystalline Cr- and Sb-codoped anatase nanoparticles. Discrete and morphologically well-defined assemblies of anatase nanoparticles sized below 100 nm × 50 nm were prepared by hydrothermal aging of aqueous solutions containing titanium alkoxide, chromium acetylacetonate, antimony acetate and triethanolamine (TEOA) as stabilizer. The as-prepared and TEOA-free doped nanoparticles showed similar crystallographic parameters and spectroscopic features. The incorporation of Cr and Sb dopant cations into the anatase nanoparticles was evaluated by Rietveld refinement of X-ray diffraction pa…

Tuning the Self-Assembly of Rectangular Amphiphilic Cruciforms

The self-assembly of a series of nonionic amphiphilic cruciforms based on the 1,2,4,5-tetrakis(phenylethynyl)benzene (TPEB) skeleton, in which the peripheral substituents have been modified to modulate the morphology of the supramolecular structures, is reported. The presence of linear paraffinic and hydrophilic chains in TPEBs 1 and 2 gives rise to two-dimensional structures of high aspect ratio. In contrast, the incorporation of dendronized hydrophilic chains results in the formation of twisted ribbons in amphiphile 3 and impedes the organized self-assembly of TPEB 4. Theoretical calculations show that the self-assembly of these amphiphiles might be initiated with the formation of π-stack…

Mesocrystalline anatase nanoparticles synthesized using a simple hydrothermal approach with enhanced light harvesting for gas-phase reaction

Mesocrystalline TiO2 nanoparticles were synthesized using a hydrothermal approach. A simple two-step procedure at low temperature (<140 °C) allowed the nucleation of primary particles sized 2–4 nm and their subsequent assembly as almost spherical aggregates sized ≈20 nm. X-ray powder diffraction (XRD), Raman and X-ray photoelectron spectroscopy (XPS) studies, and HRTEM studies confirmed anatase as the unique TiO2 crystalline phase. The mesocrystalline structure of the anatase aggregates was clearly evidenced by HRTEM and SAED results. The mesocrystalline nanopowders exhibit a mesoporous structure with a surface area and pore volume of 63.5 m2 g−1 and 0.22 cm3 g−1, respectively. Ultraviolet …

Supramolecular Polymers: Flexible Chirality in Self-Assembled N -Annulated Perylenedicarboxamides (Small 20/2017)

Synthesis and radical coupling of pyridine-bridged π-extended tetrathiafulvalene (TTF)-type donors and push–pull analogues

A new family of pi-extended TTF analogues (3a-c) and D-pi-A chromophores (5a-c), in which the electroactive units (1,3-dithiole rings and 2,2-dicyanovinyl groups) are connected through a pyridine bridge with a meta substitution pattern, is reported. The redox behavior of these compounds has been investigated by cyclic voltammetry and theoretical calculations performed at the B3P86/6-31G** level. Unlike many pi-extended TTF derivatives, the 1,3-dithiole rings in compounds 3a-c do not behave independently and two oxidation processes are observed with an anodic separation ranging from 50 to 150 mV. Calculations show that electrons are equally extracted from both dithiole rings. A biradical str…

Relacion de la persecucion que huuo en la Iglesia de Iapon y de los insignes martires que... dieron sus vidas en defensa de nuestra Santa Fè el año 1622

Sign.: ¶4, A-H4, I2 Escut xil. de la Companyia de Jesus a la port

Diskrete supramolekulare Donor-Akzeptor-Komplexe

Synthesis, properties and charge transfer complexes of covalently attached [60]fullerene-tetrathiafulvalenes

Abstract The synthesis of several fulleropyrrolidines bearing differently substitued tetrathiafulvalenes is reported. The synthetic approach used allows the introduction of ethylene spacers between the TTF and the C 60 core. Charge transfer complexes obtained from these [60]fullerene-TTF systems by reaction with tetrafluoro-tetracyano-p-quinodimethane (TCNQF 4 ) show a semiconducting behaviour; theoretical calculations predict an intramolecular CT band from the TTF moiety to the C 60 core.

Decoding the Consequences of Increasing the Size of Self-Assembling Tricarboxamides on Chiral Amplification

A complete series of experimental and theoretical investigations on the supramolecular polymerization of chiral (1 and 2) and achiral (3) oligo(phenylene ethynylene) tricarboxamides (OPE-TAs) is reported. The performance of seargents-and-soldiers (SaS) and majority rules (MR) experiments has allowed deriving a full set of thermodynamic parameters, including the helix reversal penalty (HRP) and the mismatch penalty (MMP). The results described illustrate the influence exerted by the number of stereogenic centers per monomeric unit and the temperature on the chiral amplification phenomenon. While the HRP decreases upon decreasing the number of chiral side chains, the MMP follows an opposite t…

Blue-emitting pyrene-based aggregates.

The self-assembling features and gel formation of two pyrene imidazoles are presented. The supramolecular aggregation of these synthesised molecules results in an unusual blue-monomeric emission, which is rationalized by a combined experimental and theoretical investigation.

Flexible Chirality in Self-Assembled N-Annulated Perylenedicarboxamides.

N-annulated perylenedicarboxamides 1-3 form supramolecular polymers with a strong tendency to aggregate. The bundles of fibers formed generate a spontaneous anisotropy that conditions the chiroptical features of the described molecules in solution; a strong linear dichroism effect accompanies the circular dichroism (CD) outcome. There is no influence of the point chirality existing at the side chains of 1 and 2, and these molecules present the same chiroptical features as achiral 3. Mechanical rotary stirring increases the CD response and the sign of the dichroic signal changes with the stirring direction. Theoretical calculations indicate that the self-assembly of 1-3 in helical columnar s…

Oratio in funere.

Sign.: §-§§4, A-E4.

The first spiroconjugated TTF- and TCNQ-type molecules: a new class of electroactive systems?

[Structure: see text] Spiroconjugated TTF-type electron donors (13a-c) and TCNQ-type electron acceptors (10, 11) have been prepared from spiroquinone 9. Cyclic voltammetry reveals a relatively weak accepting ability for 10 and 11, and a strong electron-donor character for 13a-c. Whereas the spiroconjugation introduces a destabilization of the LUMO for compounds 9-11, the opposite is observed for compound 13, thus justifying the redox potential values.

A new type of pi-electron donors with one dithiole unit: Substituted 7-(1,3-dithiol-2-ylidene)-7-hydrobenz[d,e]anthracenes

New electron donors 11a–c bearing only one 1,3-dithiole ring conjugated with an acene backbone have been synthesized by Wittig–Horner reactions from 7H-benz[d,e]anthracen-7-one (10) and differently substituted phosphonate esters 9a–c. The donor properties of 11 have been characterized by means of both experimental techniques and quantum chemical calculations. Cyclic voltammetry measurements on the novel compounds predict donor abilities comparable to those of TTF and BEDT-TTF. The voltammograms show a multi-stage redox behaviour with oxidation up to the trication, where the first two oxidation processes take place at very close potentials. These processes have been assigned to a simultaneou…

Impact of Molecular Size and Shape on the Supramolecular Co‐Assembly of Chiral Tricarboxamides: A Comparative Study

We report herein a comparative investigation of the chiral amplification features of a series of three families of C 3 -symmetric tricarboxamides: 1,3,5-triphenylbenzenetricarboxamides (TPBAs), benzenetricarboxamides (BTAs) and oligo(phenylene ethynylene) tricarboxamides (OPE-TAs). As previously observed for BTAs and OPE-TAs, a similar dichroic response is obtained for TPBAs decorated with three, two or only one chiral side chain bearing stereogenic centers, thus confirming the efficient transfer of point chirality to the supramolecular helical aggregates. Unlike BTAs and OPE-TAs, the chiral amplification ability of TPBAs in majority rules experiments shows a negligible dependence on the nu…

Distance Matters: Biasing Mechanism, Transfer of Asymmetry, and Stereomutation in N-Annulated Perylene Bisimide Supramolecular Polymers

International audience; The synthesis of two series of N-annulated perylene bisimides (PBIs), compounds 1 and 2, is reported, and their self-assembling features are thoroughly investigated by a complete set of spectroscopic measurements and theoretical calculations. The study corroborates the enormous influence that the distance between the PBI core and the peripheral groups exerts on the chiroptical properties and the supramolecular polymerization mechanism. Compounds 1, with the peripheral groups separated from the central PBI core by two methylenes and an ester group, form J-type supramolecular polymers in a cooperative manner but exhibit negligible chiroptical properties. The lack of cl…

N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates

The unique self-assembling features of N-annulated perylene bisimides (PBIs) 1 and 2 are reported. The stability of the aggregates of diester 1, in which no H-bonding interactions are operative, corroborates the significance of long-range van der Waals and dipole-dipole electrostatic interactions in the construction of stable supramolecular assemblies. The incorporation of amide functional groups within the N-annulated PBI in 2 stimulates pathway differentiation to achieve up to three J-type aggregates and a fourth H-type aggregate depending on the experimental conditions. The results presented demonstrate unprecedented levels of control over synthetic supramolecular self-assembly and the r…

Discrete supramolecular donor-acceptor complexes

The renewed interest in noncovalently associating electroactive molecules arises in part from the quest for new organic materials that convert solar energy into electrical/ chemical equivalents. In this context, the formation of charge-separated states is a key prerequisite. Charge-transfer events triggered by light have been studied in supramolecular donor–acceptor systems based on hydrogen bonds and coordinative metal bonds. Although many of the most widely utilized electroactive fragments feature large pconjugated surfaces, to date the use of p–p aromatic interactions has mainly been limited to the construction of semi-infinite ensembles of chromophores either to achieve charge transport…

Inside Back Cover: N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates (Angew. Chem. Int. Ed. 40/2020)

Flipping Motion To Bias the Organized Supramolecular Polymerization of N-Heterotriangulenes

Synergistic experimental and theoretical studies have allowed the disentangling of the possible pathways for the supramolecular polymerization of a series of dicyanovinyl-bridged N-heterotriangulene (NHT) derivatives bearing benzamide units with achiral (1a) and chiral (1b,c) side chains. The synthesis of these bowl-shaped, self-assembling units yields a mixture of monomeric species with C3- and C1-symmetry. Both monomeric species are able to self-assemble into different supramolecular aggregates with sufficient stability to coexist in freshly prepared solutions. The dissimilar ratio of the aggregates initially generated results in different spectroscopic features and, more specifically, in…