共 62 条
ortho-Functionalization of azobenzenes via hypervalent iodine reagents
被引:5
作者:

Di Tommaso, Ester Maria
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机构:
Stockholm Univ, Dept Organ Chem, Arrhenius Lab, Stockholm, Sweden Stockholm Univ, Dept Organ Chem, Arrhenius Lab, Stockholm, Sweden

Walther, Melanie
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h-index: 0
机构:
Univ Bremen, Inst Analyt & Organ Chem, Bremen, Germany
Univ Bremen, MAPEX Ctr Mat & Proc, Bremen, Germany Stockholm Univ, Dept Organ Chem, Arrhenius Lab, Stockholm, Sweden

Staubitz, Anne
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h-index: 0
机构:
Univ Bremen, Inst Analyt & Organ Chem, Bremen, Germany
Univ Bremen, MAPEX Ctr Mat & Proc, Bremen, Germany Stockholm Univ, Dept Organ Chem, Arrhenius Lab, Stockholm, Sweden

Olofsson, Berit
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h-index: 0
机构:
Stockholm Univ, Dept Organ Chem, Arrhenius Lab, Stockholm, Sweden Stockholm Univ, Dept Organ Chem, Arrhenius Lab, Stockholm, Sweden
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.
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收藏
页码:5047 / 5050
页数:4
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