Ultrafast photoinduced processes in subphthalocyanine electron donor-acceptor conjugates linked by a single B-N bond∥
Nieto CR, Guilleme J, Fernandez-Ariza J, Salome Rodriguez-Morgade M, Gonzalez-Rodriguez D, Torres T, Guldi DM (2012)
Publication Type: Journal article, Original article
Publication year: 2012
Journal
Original Authors: Romero-Nieto C., Guilleme J., Fernandez-Ariza J., Rodriguez-Morgade M.S., Gonzalez-Rodriguez D., Torres T., Guldi D.M.
Publisher: American Chemical Society
Book Volume: 14
Pages Range: 5656-5659
Journal Issue: 22
DOI: 10.1021/ol302632u
Abstract
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. © 2012 American Chemical Society.
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APA:
Nieto, C.R., Guilleme, J., Fernandez-Ariza, J., Salome Rodriguez-Morgade, M., Gonzalez-Rodriguez, D., Torres, T., & Guldi, D.M. (2012). Ultrafast photoinduced processes in subphthalocyanine electron donor-acceptor conjugates linked by a single B-N bond∥. Organic Letters, 14(22), 5656-5659. https://doi.org/10.1021/ol302632u
MLA:
Nieto, Carlos Romero, et al. "Ultrafast photoinduced processes in subphthalocyanine electron donor-acceptor conjugates linked by a single B-N bond∥." Organic Letters 14.22 (2012): 5656-5659.
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