Non-covalent versus covalent donoracceptor systems based on near-infrared absorbing azulenocyanines and C60 fullerene derivativesElectronic supplementary information (ESI) available: Experimental details, additional spectra and analysis data. See DOI: 10.1039/c2cc30632h
A novel supramolecular electron donoracceptor hybrid ( 21 ) and an electron donoracceptor conjugate ( 3 ), both exhibiting a remarkably shifted Q band in the NIR region of the solar spectrum, were prepared. Irradiation of the supramolecular ensemble 2 1 within the visible range leads to a nanosecond...
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| creator | Ince, Mine Hausmann, Anita Martnez-Daz, M. Victoria Guldi, Dirk M Torres, Toms |
| description | A novel supramolecular electron donoracceptor hybrid (
21
) and an electron donoracceptor conjugate (
3
), both exhibiting a remarkably shifted Q band in the NIR region of the solar spectrum, were prepared. Irradiation of the supramolecular ensemble
2
1
within the visible range leads to a nanosecond lived radicalion pair state Znazulenocyanine&z.rad;
+
C
60
&z.rad;
.
Supramolecular and covalent ZnazulenocyanineC
60
systems, which exhibit a remarkable panchromatic absorption, have been prepared and their photophysical properties studied. |
| doi_str_mv | 10.1039/c2cc30632h |
| format | Article |
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21
) and an electron donoracceptor conjugate (
3
), both exhibiting a remarkably shifted Q band in the NIR region of the solar spectrum, were prepared. Irradiation of the supramolecular ensemble
2
1
within the visible range leads to a nanosecond lived radicalion pair state Znazulenocyanine&z.rad;
+
C
60
&z.rad;
.
Supramolecular and covalent ZnazulenocyanineC
60
systems, which exhibit a remarkable panchromatic absorption, have been prepared and their photophysical properties studied.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c2cc30632h</identifier><language>eng</language><creationdate>2012-03</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Ince, Mine</creatorcontrib><creatorcontrib>Hausmann, Anita</creatorcontrib><creatorcontrib>Martnez-Daz, M. Victoria</creatorcontrib><creatorcontrib>Guldi, Dirk M</creatorcontrib><creatorcontrib>Torres, Toms</creatorcontrib><title>Non-covalent versus covalent donoracceptor systems based on near-infrared absorbing azulenocyanines and C60 fullerene derivativesElectronic supplementary information (ESI) available: Experimental details, additional spectra and analysis data. See DOI: 10.1039/c2cc30632h</title><description>A novel supramolecular electron donoracceptor hybrid (
21
) and an electron donoracceptor conjugate (
3
), both exhibiting a remarkably shifted Q band in the NIR region of the solar spectrum, were prepared. Irradiation of the supramolecular ensemble
2
1
within the visible range leads to a nanosecond lived radicalion pair state Znazulenocyanine&z.rad;
+
C
60
&z.rad;
.
Supramolecular and covalent ZnazulenocyanineC
60
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21
) and an electron donoracceptor conjugate (
3
), both exhibiting a remarkably shifted Q band in the NIR region of the solar spectrum, were prepared. Irradiation of the supramolecular ensemble
2
1
within the visible range leads to a nanosecond lived radicalion pair state Znazulenocyanine&z.rad;
+
C
60
&z.rad;
.
Supramolecular and covalent ZnazulenocyanineC
60
systems, which exhibit a remarkable panchromatic absorption, have been prepared and their photophysical properties studied.</abstract><doi>10.1039/c2cc30632h</doi><tpages>3</tpages></addata></record> |
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| source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| title | Non-covalent versus covalent donoracceptor systems based on near-infrared absorbing azulenocyanines and C60 fullerene derivativesElectronic supplementary information (ESI) available: Experimental details, additional spectra and analysis data. See DOI: 10.1039/c2cc30632h |
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