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Formation of Zwitterionic Fullerodendron Using a New DBN-Focal Dendron

A new poly(amidoamine) dendron having 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) at the focal point was synthesized. Interestingly, formation of zwitterionic fullerodendrons (λ(max) = 930 nm for C(60) and 795 nm for C(70)) were observed by Vis-NIR spectroscopy upon the reaction of C(60) or C(70) with th...

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Autores principales: Takaguchi, Yutaka, Hosokawa, Maki, Mayahara, Masatoshi, Tajima, Tomoyuki, Sasamori, Takahiro, Tokitoh, Norihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3270858/
https://www.ncbi.nlm.nih.gov/pubmed/22315557
http://dx.doi.org/10.3390/s100100613
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author Takaguchi, Yutaka
Hosokawa, Maki
Mayahara, Masatoshi
Tajima, Tomoyuki
Sasamori, Takahiro
Tokitoh, Norihiro
author_facet Takaguchi, Yutaka
Hosokawa, Maki
Mayahara, Masatoshi
Tajima, Tomoyuki
Sasamori, Takahiro
Tokitoh, Norihiro
author_sort Takaguchi, Yutaka
collection PubMed
description A new poly(amidoamine) dendron having 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) at the focal point was synthesized. Interestingly, formation of zwitterionic fullerodendrons (λ(max) = 930 nm for C(60) and 795 nm for C(70)) were observed by Vis-NIR spectroscopy upon the reaction of C(60) or C(70) with the DBN-focal dendron. In particular, the C(70) anion was effectively stabilized by the site isolation effect of the dendritic wedge. The half-life of fullerodendron 12b having C(70) anion at the focal point reaches 7,345 min, which is 20 times longer than that of complex between C(60) and pristine DBN. Furthermore, in order to confirm the structure of the zwitterionic complex, fullerodendron 12a was reprecipitated from benzonitrile/1,2,4-trimethylbenzene, and was observed using IR spectroscopy and APPI-MS.
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spelling pubmed-32708582012-02-07 Formation of Zwitterionic Fullerodendron Using a New DBN-Focal Dendron Takaguchi, Yutaka Hosokawa, Maki Mayahara, Masatoshi Tajima, Tomoyuki Sasamori, Takahiro Tokitoh, Norihiro Sensors (Basel) Article A new poly(amidoamine) dendron having 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) at the focal point was synthesized. Interestingly, formation of zwitterionic fullerodendrons (λ(max) = 930 nm for C(60) and 795 nm for C(70)) were observed by Vis-NIR spectroscopy upon the reaction of C(60) or C(70) with the DBN-focal dendron. In particular, the C(70) anion was effectively stabilized by the site isolation effect of the dendritic wedge. The half-life of fullerodendron 12b having C(70) anion at the focal point reaches 7,345 min, which is 20 times longer than that of complex between C(60) and pristine DBN. Furthermore, in order to confirm the structure of the zwitterionic complex, fullerodendron 12a was reprecipitated from benzonitrile/1,2,4-trimethylbenzene, and was observed using IR spectroscopy and APPI-MS. Molecular Diversity Preservation International (MDPI) 2010-01-14 /pmc/articles/PMC3270858/ /pubmed/22315557 http://dx.doi.org/10.3390/s100100613 Text en ©2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/)
spellingShingle Article
Takaguchi, Yutaka
Hosokawa, Maki
Mayahara, Masatoshi
Tajima, Tomoyuki
Sasamori, Takahiro
Tokitoh, Norihiro
Formation of Zwitterionic Fullerodendron Using a New DBN-Focal Dendron
title Formation of Zwitterionic Fullerodendron Using a New DBN-Focal Dendron
title_full Formation of Zwitterionic Fullerodendron Using a New DBN-Focal Dendron
title_fullStr Formation of Zwitterionic Fullerodendron Using a New DBN-Focal Dendron
title_full_unstemmed Formation of Zwitterionic Fullerodendron Using a New DBN-Focal Dendron
title_short Formation of Zwitterionic Fullerodendron Using a New DBN-Focal Dendron
title_sort formation of zwitterionic fullerodendron using a new dbn-focal dendron
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3270858/
https://www.ncbi.nlm.nih.gov/pubmed/22315557
http://dx.doi.org/10.3390/s100100613
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