Radhakrishnan SG, Guldi DM, Perez EM, Perez I, Bietti M, Martin N (2010)
Publication Type: Journal article, Original article
Publication year: 2010
Original Authors: Radhakrishnan S.G., Guldi D.M., Perez E.M., Perez I., Bietti M., Martin N.
Publisher: Taylor & Francis: STM, Behavioural Science and Public Health Titles / Taylor & Francis
Book Volume: 63
Pages Range: 2939-2948
DOI: 10.1080/00958972.2010.500666
Charge-transfer complex formation by a tuning-fork shaped π-extended tetrathiafulvalene-based molecule, which acts as molecular catcher for C in a variety of solvents upon photoexcitation, has been explored. An increase in 2-[9-(1, 3-dithiol-2-ylidene)anthracen-10(9H)-ylidene]-1, 3-dithiole unit creates an easy-chair like conformation accommodating C60, which leads to a binding constant and lifetime of radical ion pair state of 2.23 × 10 (mol L ) and 4.8 ps in ortho-dichlorobenzene. © 2010 Taylor & Francis.
APA:
Radhakrishnan, S.G., Guldi, D.M., Perez, E.M., Perez, I., Bietti, M., & Martin, N. (2010). Threefold exTTF-based Buckycatcher. Journal of Coordination Chemistry, 63, 2939-2948. https://doi.org/10.1080/00958972.2010.500666
MLA:
Radhakrishnan, Shankara Gayathri, et al. "Threefold exTTF-based Buckycatcher." Journal of Coordination Chemistry 63 (2010): 2939-2948.
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