THE STEREOCHEMISTRY OF THE TRINAPHTHYL-TERRYLENE CONVERSION

被引：8

作者：

ANTON, U ^{[1
]}

ADAM, M ^{[1
]}

WAGNER, M ^{[1
]}

ZHOU, QL ^{[1
]}

MULLEN, K ^{[1
]}

机构：

[1] MAX PLANCK INST POLYMER RES,ACKERMANNWEG 10,W-6500 MAINZ,GERMANY

来源：

CHEMISCHE BERICHTE-RECUEIL | 1993年 / 126卷 / 02期

关键词：

STERIC STRAIN; ATROPIC ISOMERISM; TRINAPHTHYL; TERRYLENE;

D O I：

10.1002/cber.19931260231

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Alkylated terrylenes can be synthesized by a twofold cyclization of an appropriately substituted trinaphthyl[1,11]. In this paper, we consider a special case. The alkyl substitution in the starting material 1 strongly affects the interplanar angle between the naphthalene moieties. After cyclization, the substituents are positioned in the sterically crowded bay region of the title structure 2. The influence of the steric strain on the reactivity of 1 and on the stability of the resulting hydrocarbon 2 is investigated. Special emphasis is placed on the crystal structures of 1 and 2.

引用

页码：517 / 521

页数：5

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