An NMR investigation of the merocyanine dyes generated by protolysis of some novel spironaphthopyranoindoles

被引：25

作者：

Gabbutt, CD ^{[1
]}

Hepworth, JD ^{[1
]}

Heron, BM ^{[1
]}

机构：

[1] Univ Hull, Dept Chem, Hull HU6 7RX, N Humberside, England

来源：

DYES AND PIGMENTS | 1999年 / 42卷 / 01期

关键词：

photochromism; merocyanine dyes; nmr spectroscopy; synthesis; spiroindolinonaphthopyran (NIPS); protolysis;

D O I：

10.1016/S0143-7208(99)00007-8

中图分类号：

O69 [应用化学];

学科分类号：

081704 ;

摘要：

Two novel amino-substituted spiroindolinonaphthopyrans have been synthesised. Whilst these compounds exhibit no observable photochromic properties at ambient temperature, protonation gives stable, intensely coloured dyes. H-1 nmr spectroscopy has been used to establish the configuration of these dyes. (C) 1999 Elsevier Science Ltd. All rights reserved.

引用

页码：35 / 43

页数：9

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