Modification of fulleropyrazolines modulates their cleavage by light
Author:
Affiliation:
1. Chemistry Research Laboratory
2. University of Oxford
3. Oxford, UK
Abstract
The tuned photocleavage of fulleropyrazolines unveils potential for controlled release of biologically-relevant molecules or payloads.
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/2014/CC/C4CC03859B
Reference34 articles.
1. Pyrazolinofullerenes: a less known type of highly versatile fullerene derivatives
2. Excited-State Properties of C60 Fullerene Derivatives
3. C60-Based Triads with Improved Electron-Acceptor Properties: Pyrazolylpyrazolino[60]fullerenes
4. Synthesis and Photophysical Properties of a Pyrazolino[60]fullerene with Dimethylaniline Connected by an Acetylene Linkage
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1. Cyclic Voltammetric Study of 3,5-Diaryl-1-phenyl-2-pyrazolines;The Journal of Physical Chemistry A;2019-03-05
2. New pyrazolino and pyrrolidino[60]fullerenes: the introduction of the hydrazone moiety for the formation of metal complexes;Journal of Physical Organic Chemistry;2016-07-13
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