A DIELS-ALDER ADDUCT OF C-60 CONTAINING HYDROXYQUINONE FUNCTIONALITIES

W  BIDELL; R E  DOUTHWAITE; M L H  GREEN; A H H  STEPHENS; J F C  TURNER

A DIELS-ALDER ADDUCT OF C-60 CONTAINING HYDROXYQUINONE FUNCTIONALITIES

W BIDELL, R E DOUTHWAITE, M L H GREEN, A H H STEPHENS, J F C TURNER

Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

Two new Diels-Alder adducts of C-60 have been prepared from 1,3-diphenylisobenzofuran and the ortho-quinodimethane generated from 1,4-dihydroxy-2,3-bis(bromomethyl)anthraquinone: the dihydroxy anthraquinone-C-60 adduct readily undergoes deprotonation to give the corresponding dianion.

Original language	English
Pages (from-to)	1641-1642
Number of pages	2
Journal	JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS
Issue number	14
Publication status	Published - 21 Jul 1994

Keywords

BUCKMINSTERFULLERENE
CYCLOPENTADIENE
QUINODIMETHANE
DERIVATIVES
FULLERENES
C60

Cite this

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title = "A DIELS-ALDER ADDUCT OF C-60 CONTAINING HYDROXYQUINONE FUNCTIONALITIES",

abstract = "Two new Diels-Alder adducts of C-60 have been prepared from 1,3-diphenylisobenzofuran and the ortho-quinodimethane generated from 1,4-dihydroxy-2,3-bis(bromomethyl)anthraquinone: the dihydroxy anthraquinone-C-60 adduct readily undergoes deprotonation to give the corresponding dianion.",

keywords = "BUCKMINSTERFULLERENE, CYCLOPENTADIENE, QUINODIMETHANE, DERIVATIVES, FULLERENES, C60",

author = "W BIDELL and DOUTHWAITE, {R E} and GREEN, {M L H} and STEPHENS, {A H H} and TURNER, {J F C}",

year = "1994",

month = jul,

day = "21",

language = "English",

pages = "1641--1642",

journal = "JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS",

issn = "0022-4936",

publisher = "Chemical Society",

number = "14",

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T1 - A DIELS-ALDER ADDUCT OF C-60 CONTAINING HYDROXYQUINONE FUNCTIONALITIES

AU - BIDELL, W

AU - DOUTHWAITE, R E

AU - GREEN, M L H

AU - STEPHENS, A H H

AU - TURNER, J F C

PY - 1994/7/21

Y1 - 1994/7/21

N2 - Two new Diels-Alder adducts of C-60 have been prepared from 1,3-diphenylisobenzofuran and the ortho-quinodimethane generated from 1,4-dihydroxy-2,3-bis(bromomethyl)anthraquinone: the dihydroxy anthraquinone-C-60 adduct readily undergoes deprotonation to give the corresponding dianion.

AB - Two new Diels-Alder adducts of C-60 have been prepared from 1,3-diphenylisobenzofuran and the ortho-quinodimethane generated from 1,4-dihydroxy-2,3-bis(bromomethyl)anthraquinone: the dihydroxy anthraquinone-C-60 adduct readily undergoes deprotonation to give the corresponding dianion.

KW - BUCKMINSTERFULLERENE

KW - CYCLOPENTADIENE

KW - QUINODIMETHANE

KW - DERIVATIVES

KW - FULLERENES

KW - C60

M3 - Article

SN - 0022-4936

SP - 1641

EP - 1642

JO - JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS

JF - JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS

IS - 14

ER -