0000000000021348

AUTHOR

Francis D'souza

showing 5 related works from this author

Metallomacrocycles with metalmetal bonds: synthesis, characterization and electrochemistry of [(P)SnRe(CO)5]BF4 and [{(P)Sn}2Re(CO)4]BF4 derivatives…

1996

Abstract The synthesis and characterization of bimetallic and trimetallic porphyrins of the type [(P)SnRe(CO) 5 ]BF 4 and [{(P)Sn} 2 Re(CO) 4 ]BF 4 are reported where P is the dianion of tetra- p -tolyporphyrin (TpTP) or tetra- m -tolyporphyrin (TmTP). These metal-metal bonded complexes were synthesized by reaction of Re 2 (CO) 10 with the corresponding (P)SnCl 2 derivatives in 1,2-dichlorobenzene followed by a reaction with NaBF 4 or TBABF 4 in toluene to give the BF − 4 salt. Each compound was characterized by a variety of spectroscopic and electrochemical techniques while the structures were assigned on the basis of FAB mass spectral data and by comparison of their physicochemical proper…

biologyInorganic chemistryConjugated systembiology.organism_classificationElectrochemistryCleavage (embryo)PorphyrinMedicinal chemistryTolueneRedoxInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryTetraPhysical and Theoretical ChemistryBimetallic stripInorganica Chimica Acta
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Face-to-face held Pacman type porphyrin-fullerene dyads: design, synthesis, charge transfer interactions and photophysical studies

2008

Pacman-type face-to-face zinc-porphyrin-fullerene dyads have been newly synthesized and studied. Owing to the close proximity of the donor and acceptor entities, strong pi-pi intramolecular interactions between the porphyrin and fullerene entities resulted in modulating the spectral and electrochemical properties of the dyads. New absorption and emission bands that correspond to the charge-transfer interactions were observed in the near-IR region. Time-resolved transient absorption studies revealed efficient photoinduced electron transfer from the singlet excited porphyrin to the fullerene entity. The rate constants for photoinduced electron transfer are analyzed in terms of the Marcus theo…

Models MolecularFullereneMagnetic Resonance SpectroscopyPorphyrinsTime FactorsPhotochemistryporphyrinoids010402 general chemistryPhotochemistry01 natural sciencesCatalysisPhotoinduced electron transferElectron Transportchemistry.chemical_compoundElectron transfer[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganometallic CompoundsComputingMilieux_MISCELLANEOUSphotosynthesisMolecular Structure010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrycharge transferfullerenesGeneral Chemistryelectron transferAcceptorPorphyrin0104 chemical sciencesMarcus theoryZincSpectrometry FluorescenceModels ChemicalExcited stateIntramolecular forceSpectrophotometry UltravioletDimerization
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Effect of Peripheral Substitution and Extended Conjugation on the Redox Potentials of Nickel Porphycenes

1996

Eight different nickel porphycenes bearing substituents on the pyrrole β and/or ethylenic carbon positions of the macrocycle were investigated as to their redox properties in benzonitrile containin...

Inorganic ChemistryNickelBenzonitrilechemistry.chemical_compoundchemistrySubstitution (logic)chemistry.chemical_elementPhysical and Theoretical ChemistryPhotochemistryCarbonRedoxPyrroleInorganic Chemistry
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Self-Assembly-Directed Organization of a Fullerene–Bisporphyrin into Supramolecular Giant Donut Structures for Excited-State Charge Stabilization

2021

Functional materials composed of spontaneously self-assembled electron donor and acceptor entities capable of generating long-lived charge-separated states upon photoillumination are in great demand as they are key in building the next generation of light energy harvesting devices. However, creating such well-defined architectures is challenging due to the intricate molecular design, multistep synthesis, and issues associated in demonstrating long-lived electron transfer. In this study, we have accomplished these tasks and report the synthesis of a new fullerene–bis-Zn-porphyrin e-bisadduct by tether-directed functionalization of C60 via a multistep synthetic protocol. Supramolecular oligom…

FullereneSupramolecular structures and assembliesChemistrySupramolecular chemistryGeneral ChemistryBiochemistryAcceptorArticleCatalysisElectron transferColloid and Surface ChemistryCharge transferChemical structureChemical physicsExcited stateEnergy levelMoleculePyrrolesSelf-assemblyMolecular structure
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Synthesis and Electrochemical Reactivity of sigma-Bonded and N-Substituted Cobalt Porphycenes.

1998

The first synthesis and characterization of sigma-bonded and N-substituted cobalt porphycenes is reported. The investigated compounds are represented as (Pc)Co(R) and (N-CH(3)OEPc)CoCl, where R is CH(3) or C(6)H(5), Pc is the dianion of 2,3,6,7,12,13,16,17-octaethylporphycene (OEPc), 2,7,12,17-tetrapropylporphycene (TPrPc), or 2,7,12,17-tetraethyl-3,6,13,16-tetramethylporphycene (EtioPc), N-CH(3)OEPc is the monoanion of N-methyl-2,3,6,7,12,13,16,17-octaethylporphycene. Each sigma-bonded (Pc)Co(R) derivative can be reversibly reduced or oxidized by two electrons, but a slow migration of the sigma-bonded R group occurs following electrogeneration of [(Pc)Co(R)](+)()(*)() leading, as a final p…

Inorganic Chemistrychemistry.chemical_compoundReduced productchemistryStereochemistrychemistry.chemical_elementReactivity (chemistry)Physical and Theoretical ChemistryElectrochemistryMedicinal chemistryCobaltDerivative (chemistry)Inorganic chemistry
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