Ultrafast Photoinduced Processes in Subphthalocyanine Electron Donor–Acceptor Conjugates Linked by a Single B–N Bond

We have prepared two different subphthalocyanine conjugates by linking these macrocycles either to an electron-accepting perylene diimide or to an electron-donating phenothiazine through a single B–N covalent bond. The short spacing between the two active building blocks results in ultrafast photoin...

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Bibliographic Details
Published inOrganic letters Vol. 14; no. 22; pp. 5656 - 5659
Main Authors Romero-Nieto, Carlos, Guilleme, Julia, Fernández-Ariza, Javier, Rodríguez-Morgade, M. Salomé, González-Rodríguez, David, Torres, Tomás, Guldi, Dirk M
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 16.11.2012
Amer Chemical Soc
Subjects
Chemistry
Chemistry, Organic
Imides
Macrocyclic Compounds - chemistry
Molecular Conformation
Molecular Structure
Perylene - analogs & derivatives
Phenothiazines - chemistry
Photochemical Processes
Physical Sciences
Science & Technology
ENERGY-TRANSFER
SEPARATION
CHARGE-TRANSFER
DYADS
FULLERENE
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Summary:We have prepared two different subphthalocyanine conjugates by linking these macrocycles either to an electron-accepting perylene diimide or to an electron-donating phenothiazine through a single B–N covalent bond. The short spacing between the two active building blocks results in ultrafast photoinduced electron-transfer reactions.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1523-7060
1523-7052
DOI:10.1021/ol302632u