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Synthesis of New Dendrimers Based on 6,8-Dinitroquinazoline and 3,5-Dimercaptobenzyl Blocks

Published online by Cambridge University Press:  21 March 2011

Hideki Miki ,
Shiyoshi Yokoyama  and
Shinro Mashiko
Hideki Miki
Affiliation:
Nanotechnology Section, Kansai Advanced Research Center, Communications Research Laboratory, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe 651-2492, JAPAN Fax:+81-78-969-2259, E-mail:himiki@crl.go.jp
Shiyoshi Yokoyama
Affiliation:
Nanotechnology Section, Kansai Advanced Research Center, Communications Research Laboratory, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe 651-2492, JAPAN Fax:+81-78-969-2259, E-mail:himiki@crl.go.jp
Shinro Mashiko
Affiliation:
Nanotechnology Section, Kansai Advanced Research Center, Communications Research Laboratory, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe 651-2492, JAPAN Fax:+81-78-969-2259, E-mail:himiki@crl.go.jp
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Abstract

Two types of core-shell structured dendrimer, 2,4-bis-{3,5-bis-[3,5-bis-(3,5-di-tert- butylbenzylthio)benzylthio]benzyloxy}-6,8-dinitroquinazoline (7a) and 2,4-bis-{3,5-bis-[3,5-bis- (3,5-di-tertbutylbenzyloxy)benzyloxy]benzyloxy}-6,8-dinitroquinazoline (7b) as a referential compound were synthesized. These compounds consist of a 6,8-dinitroquinazoline ring as the functional unit and a 3,5-dimercaptobenzyl or a 3,5-dihydroxybenzyl group as the dendritic unit. In order to protect the sulfur atom in dendrimer (7a) from the oxidation reaction, a 3,5-di-tert- butylbenzyl group was designed as the outer-most unit. The synthesized dendrimer containing 3,5-dimercaptobenzyl blocks (7a) is completely novel, and is interesting as a photoelectronic material to examine what kind of influence the d-orbital electron properties give to the whole molecule.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 660: Symposia JJ – Organic Electronic & Photonic Materials and Devices , 2000 , JJ5.32
Copyright
Copyright © Materials Research Society 2001

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References

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