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Meso Position (meso + position)
Selected AbstractsSynthetic Potentials of Heptamethine Merocyanine Dyes Containing an Active Chlorine Atom: Reactivity towards NucleophilesEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 29 2009Tzveta Gospodova Abstract The reactivity of heptamethine merocyanine dyes that contain an active chlorine atom at a meso position of the polymethine chain towards nucleophiles is investigated for the first time. The reactivity differs completely from that of cationic cyanine dyes and is consistent with a concerted SNAr addition,elimination mechanism. This mechanism is additionally supported by the performed DFT calculations in the gas phase and in solution. The observed dependence of the reaction on the type of the nucleophilic agents is discussed in terms of Pearson's theory. Additional diversification of and improvement in the stability of the ramified merocyanines is achieved in reactions with methyl-substituted quaternary salts of nitrogen-containing heterocycles. The photophysical characteristics of the novel dyes are reported and compared with those of the parent merocyanine.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Stable Ion and Electrophilic Substitution (Nitration and Bromination) Study of A-Ring Substituted Phenanthrenes: Novel Carbocations and Substituted Derivatives; NMR, X-ray Analysis, and Comparative DNA BindingEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 3 2007Cédric Brulé Abstract Persistent carbocations were generated from five A-ring mono- and di-substituted phenanthrenes [3-OMe; 4-OMe, 1,3-bis(OMe), 2,4-bis(OMe), and 1,3-bis(Me)]. In all cases protonation occurs in the A-ring, ortho/para relative to methoxy or methyl substituent(s). Complete NMR assignments of the resulting carbocations are reported and their charge delocalization modes are discussed. Mild nitration (with 20,50,% aqueous HNO3 at ,10 °C or at room temp.) and bromination (NBS/MeCN/room temp.) of these substrates resulted in the synthesis of several novel mononitro-/dinitro- as well as monobromo/dibromo derivatives, including those with nitro or bromo substituent in the bay-region. Correspondence between the site of attack in low-temperature protonation study and nitro substitution in ambient mild nitrations are examined. Complete NMR assignments for the new derivatives are reported as well as X-ray structures for 2,4-dimethoxy-1-nitro- and 1,3-dimethyl-4-nitrophenanthrenes. A comparative DNA binding study with MCF cells on three of the synthesized mononitro and one dinitro derivative showed that 1,3-dimethyl-9-nitro- (nitro at the meso position), 3-methoxy-4-nitro- (nitro in bay-region), and 1,3-dimethoxy-4,9-dinitrophenanthrenes (nitro in both meso and bay-regions) formed DNA adducts. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Novel Zinc Porphyrin Sensitizers for Dye-Sensitized Solar Cells: Synthesis and Spectral, Electrochemical, and Photovoltaic PropertiesCHEMISTRY - A EUROPEAN JOURNAL, Issue 6 2009Cheng-Wei Lee Abstract Novel meso - or ,-derivatized porphyrins with a carboxyl group have been designed and synthesized for use as sensitizers in dye-sensitized solar cells (DSSCs). The position and nature of a bridge connecting the porphyrin ring and carboxylic acid group show significant influences on the spectral, electrochemical, and photovoltaic properties of these sensitizers. Absorption spectra of porphyrins with a phenylethynyl bridge show that both Soret and Q,bands are red-shifted with respect to those of porphyrin 6. This phenomenon is more pronounced for porphyrins 3 and 4, which have a ,-conjugated electron-donating group at the meso position opposite the anchoring group. Upon introduction of an ethynylene group at the meso position, the potential at the first oxidation alters only slightly whereas that for the first reduction is significantly shifted to the positive, thus indicating a decreased HOMO,LUMO gap. Quantum-chemical (DFT) results support the spectroelectrochemical data for a delocalization of charge between the porphyrin ring and the amino group in the first oxidative state of diarylamino-substituted porphyrin 5, which exhibits the best photovoltaic performance among all the porphyrins under investigation. From a comparison of the cell performance based on the same TiO2 films, the devices made of porphyrin 5 coadsorbed with chenodeoxycholic acid (CDCA) on TiO2 in ratios [5]/[CDCA]=1:1 and 1:2 have efficiencies of power conversion similar to that of an N3 -based DSSC, which makes this green dye a promising candidate for colorful DSSC applications. [source] Single-Step Electron Transfer on the Nanometer Scale: Ultra-Fast Charge Shift in Strongly Coupled Zinc Porphyrin,Gold Porphyrin DyadsCHEMISTRY - A EUROPEAN JOURNAL, Issue 11 2008Jérôme Fortage Dr. Abstract The synthesis, electrochemical properties, and photoinduced electron transfer processes of a series of three novel zinc(II),gold(III) bisporphyrin dyads (ZnPSAuP+) are described. The systems studied consist of two trisaryl porphyrins connected directly in the meso position via an alkyne unit to tert -(phenylenethynylene) or penta(phenylenethynylene) spacers. In these dyads, the estimated center to center interporphyrin separation distance varies from 32 to 45,Å. The absorption, emission, and electrochemical data indicate that there are strong electronic interactions between the linked elements, thanks to the direct attachment of the spacer on the porphyrin ring through the alkyne unit. At room temperature in toluene, light excitation of the zinc porphyrin results in almost quantitative formation of the charge shifted state .+ZnPSAuP., whose lifetime is in the order of hundreds of picoseconds. In this solvent, the charge-separated state decays to the ground state through the intermediate population of the zinc porphyrin triplet excited state. Excitation of the gold porphyrin leads instead to rapid energy transfer to the triplet ZnP. In dichloromethane the charge shift reactions are even faster, with time constants down to 2,ps, and may be induced also by excitation of the gold porphyrin. In this latter solvent, the longest charge-shifted lifetime (,=2.3,ns) was obtained with the penta-(phenylenethynylene) spacer. The charge shift reactions are discussed in terms of bridge-mediated super-exchange mechanisms as electron or hole transfer. These new bis-porphyrin arrays, with strong electronic coupling, represent interesting molecular systems in which extremely fast and efficient long-range photoinduced charge shift occurs over a long distance. The rate constants are two to three orders of magnitude larger than for corresponding ZnPAuP+ dyads linked via meso -phenyl groups to oligo-phenyleneethynylene spacers. This study demonstrates the critical impact of the attachment position of the spacer on the porphyrin on the electron transfer rate, and this strategy can represent a useful approach to develop molecular photonic devices for long-range charge separations. [source] Synthesis and Physicochemical Characterization of Bis(macrocycles) Involving a Porphyrin and a meso -Substituted Corrole , X-ray Crystal Structure of a [(Free-base porphyrin),corrole]bis(pyridine)cobalt ComplexEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 6 2005Jean-Michel Barbe Abstract A very efficient, simple synthesis of face-to-face porphyrin,corrole free-bases bearing substituents at the meso positions of the corrole ring is reported. Starting from the (porphyrin,aldehyde)zinc species 1Zn, porphyrin,corrole free-bases (3M, 3C) are obtained in two steps, in fairly good yields (40,43,%), compared to 11 steps for their corrole ,-pyrrole-substituted counterparts. Moreover, the possibility to directly synthesize the free-base (porphyrin,corrole)cobalt complex (5M or 5C) allows for the further preparation of heterodimetallic derivatives. Crystals of the bis(pyridine) adduct of 5M have been grown; the molecular structure clearly shows that the two pyridine molecules are coordinated to the cobalt ion in endo and exo positions, leading to an open-mouth geometry of the bis(macrocycle). The structure of 5M(py)2also shows intermolecular ,,, interactions along the [1,0,0] direction, leading to stacking of the complexes. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source] | ||||||||||