Fulleropillar[4]arene: The Synthesis and Complexation Properties

A multihydroquinone ether dialdehyde derivative 2 was incidentally obtained through an unexpected ring opening of pillar[4]­arene[1]­quinone 1. And the Prato reaction of 2 with [60]­fullerene led to [60]­fullerene bisadducts, from which trans-4 cyclic regioisomer 3 was isolated and characterized. Th...

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Published inOrganic letters Vol. 22; no. 6; pp. 2118 - 2123
Main Authors Mi, Yan, Yao, Jiabin, Ma, Jingyu, Dai, Ling, Xiao, Chao, Wu, Wanhua, Yang, Cheng
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 20.03.2020
Amer Chemical Soc
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Summary:A multihydroquinone ether dialdehyde derivative 2 was incidentally obtained through an unexpected ring opening of pillar[4]­arene[1]­quinone 1. And the Prato reaction of 2 with [60]­fullerene led to [60]­fullerene bisadducts, from which trans-4 cyclic regioisomer 3 was isolated and characterized. The fulleropillar[4]­arene 3 showed a larger cavity and can accommodate a viologen derivative C 12 V 2+ with a much stronger affinity than permethyl pillar[5]­arene (MP5) and pillar[4]­arene[1]­quinone 1.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.9b04607