ortho-Functionalization of azobenzenes via hypervalent iodine reagents

被引:4
|
作者
Di Tommaso, Ester Maria [1 ]
Walther, Melanie [2 ,3 ]
Staubitz, Anne [2 ,3 ]
Olofsson, Berit [1 ]
机构
[1] Stockholm Univ, Dept Organ Chem, Arrhenius Lab, Stockholm, Sweden
[2] Univ Bremen, Inst Analyt & Organ Chem, Bremen, Germany
[3] Univ Bremen, MAPEX Ctr Mat & Proc, Bremen, Germany
基金
瑞典研究理事会;
关键词
ONE-POT SYNTHESIS; DIARYLIODONIUM SALTS; ARYLATION; EFFICIENT; ACID; FLUOROAZOBENZENES; PHOTOSWITCHES; ARENES; SCOPE;
D O I
10.1039/d3cc01060k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
ortho-Functionalized azobenzenes are much sought after molecular switches, as they may be tuned to absorb in the visible range of light and the (Z)-isomers can have high thermal half-lives. To enable straightforward access to these targets, we have developed a synthetic route via novel ortho-substituted azobenzene-functionalized diaryliodonium salts. Selective transfer of the azobenzene moiety to O-, N-, C- and S-nucleophiles under mild, transition metal-free conditions gives access to an unprecedented range of ortho-substituted azobenzenes. The photoswitching properties of the reagents were investigated and the structure was determined by X-ray crystallography.
引用
收藏
页码:5047 / 5050
页数:4
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