Scavenging of intermediates formed in photolysis of α-diazocarbonyl compounds and hydroxycyclopropenones.: Implication on the mechanism of the photo-Wolff reaction

被引：30

作者：

Chiang, Y ^{[1
]}

Kresge, AJ ^{[1
]}

Popik, VV ^{[1
]}

机构：

[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1999年 / 121卷 / 25期

关键词：

D O I：

10.1021/ja9906406

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The question of whether alpha-carbonylcarbene intermediates are formed as ketene precursors in the photo-Wolff reaction of alpha-diazocarbonyl compounds was addressed by comparing pyridine scavenging of transients generated by laser flash photolysis of benzoyldiazomethane and 1-naphthoyldiazomethane with pyridine scavenging of transients formed by flash photolysis of the corresponding arylhydroxycyclopropenones. The rate laws for the scavenging process in the two different photoreactions in aqueous solution were found to be exactly the same, and since ketene intermediates are common to both reactions but alpha-carbonylcarbenes are not, the transients were thus identified as ketenes. Formation of these ketene intermediates in the photo-Wolff reaction took place within the duration of the laser pulse (ca. 20 ns), and alpha-carbonylcarbene intermediates, if formed at all, must have lifetimes shorter than this.

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页码：5930 / 5932

页数：3

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