Spin chemistry investigation of peculiarities of photoinduced electron transfer in donor-acceptor linked system

Photoinduced intramolecular electron transfer in linked systems, (R,S)- and (S,S)-naproxen-N-methylpyrrolidine dyads, has been studied by means of spin chemistry methods [magnetic field effect and chemically induced dynamic nuclear polarization (CIDNP)]. The relative yield of the triplet state of th...

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Detalhes bibliográficos
Autores: Magin, I.M., Polyakov, N.E., Khramtsova, E.A., Kruppa, A.I., Stepanov, A., Purtov, P.A., Leshina, T.V., Tsentalovich, Yu.T., Miranda Alonso, Miguel Ángel, Nuin Plá, Neus Edurne, Marín García, Mª Luisa|||0000-0002-9789-8894
Tipo de documento: artigo
Data de publicação:2011
País:España
Recursos:Universitat Politècnica de València (UPV)
Repositório:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglês
OAI Identifier:oai:riunet.upv.es:10251/47423
Acesso em linha:https://riunet.upv.es/handle/10251/47423
Access Level:Acceso aberto
Palavra-chave:Radical-ion-pairs
External magnetic-field
Laser Flash-Photolysis
Time-resolved cidnp
Naphthalene-amine dyads
Geminate recombination
Polar-solvents
NMR detection
Fluorescence
Photochemistry
QUIMICA ORGANICA
QUIMICA ANALITICA
Descrição
Resumo:Photoinduced intramolecular electron transfer in linked systems, (R,S)- and (S,S)-naproxen-N-methylpyrrolidine dyads, has been studied by means of spin chemistry methods [magnetic field effect and chemically induced dynamic nuclear polarization (CIDNP)]. The relative yield of the triplet state of the dyads in different magnetic field has been measured, and dependences of the high-field CIDNP of the N-methylpyrrolidine fragment on solvent polarity have been investigated. However, both (S,S)- and (R,S)-enantiomers demonstrate almost identical CIDNP effects for the entire range of polarity. It has been demonstrated that the main peculiarities of photoprocesses in this linked system are connected with the participation of singlet exciplex alongside with photoinduced intramolecular electron transfer in chromophore excited state quenching.