THIOPYRYLIUM, SELENOPYRYLIUM, AND TELLUROPYRYLIUM SALTS

被引:42
作者
DODDI, G [1 ]
ERCOLANI, G [1 ]
机构
[1] UNIV ROMA LA SAPIENZA, DIPARTIMENTO CHIM, I-00185 ROME, ITALY
来源
ADVANCES IN HETEROCYCLIC CHEMISTRY, VOL 60 | 1994年 / 60卷
关键词
D O I
10.1016/S0065-2725(08)60182-8
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This chapter deals with thiopyrylium, selenopyrylium, and telluropyrylium salts. These compounds are considered the parent structures of an important class of six-membered heteroaromatic cations. It is observed that the reactivity of thiopyrylium salts resembles that of pyrylium salts with two notable differences— namely, the lesser tendency of 2H adducts formed on nucleophilic attack to undergo ring opening and the ability of sulfur to accommodate more than eight electrons in its valence shell, leading, in some cases, to the formation of thiabenzene derivatives. The chapter also describes the structural and physical properties, the methods of synthesis, the reactions, and the practical uses of these pyrylium salts. There are large number of patents and applicative studies making use of a chalcogenopyrylium salt. Most applications of chalcogenopyrylium salts exploit their photophysical and photochemical properties, and principally regard photographic and reprographic technologies. Another important application of chalcogenopyrylium salts is as polymerization and crosslinking photoinitiators, especially in the preparation of photoresists, printing plates, and photosensitive compositions for laser imaging. © 1994, Academic Press Inc.
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页码:65 / 195
页数:131
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