Triplet Quenching by tert-Butyl Hydroperoxide

DOI: 10.1021/ja00349a042

Source and publish data:

Journal of the American Chemical Society p. 3605 - 3609 (1983)

Update date:2022-08-16

Topics:

Authors:

Stewart, Laura C.

Carlsson, D. J.

Wiles, D. M.

Scainano, J. C.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/ja00349a042

Laser flash photolysis studies show that tert-butyl hydroperoxide is an excellent quencher.For example, the rate constants for benzophenone and phenanthrene in benzene at 300 K are 1.8 x 10⁸ and 2.3 x 10⁷ M^-1 s^{-1
View More}

Full text of DOI:10.1021/ja00349a042

Products guided by the article

Product name:Methyl, hydroxy(4-methylphenyl)phenyl-

Cas No:145191-23-7

R&D Labs maybe for 145191-23-7

Jiande City Silibase Silicone New Material Manufacture Co., Ltd.

Contact:15967177856

Address:Genglou Industrial Development Area
Changsha Botaniex Inc.

Contact:(86) 731 88718666

Address:Room 1222, Unit 4, Building B, Shangcheng, No.47, Kaiyuan East Road.
Allicon Pharmaceuticals,Inc.

Contact:+86-519-86339586，13584329896

Address:Changzhou Scientific and Education Park
Xinchang Yueding Chemical Co., Ltd.

Contact:86-571-56926323

Address:NO.90 BEIMENCHENGWAI CHENGGUAN TOWN XINCHANG
changsha chenjin chemical technology co.,LtD(expird)

Contact:86-731-84451263

Address:Room 201/217-218, 101 Jingyuan Electronic Technology Co.,Ltd. Testing Center, No.69, Lufeng Road, High-tech Development Zone, Changsha, China

Relevant to this article

Doi:10.1039/C19660000129
()
Thermal and photochemical reactions of steroidal α-azido ketones

Doi:10.1139/v92-305
(1992)
Gallium Hydrides and O/N-Donors as Tunable Systems in C?F Bond Activation

Doi:10.1002/asia.201801030
(2018)
C-C bond formation via 1,2-addition of a tert-butylzinc reagent and carbonyls across conjugated dienes

Doi:10.1039/c3nj00992k
(2014)
Synthesis of ruthenium N-heterocyclic carbene complexes and their catalytic activity for β-alkylation of tertiary cyclic amines

Doi:10.1016/j.jorganchem.2015.10.011
(2015)
Chiral synthesis VIA organoboranes. 26. An efficient synthesis of isoprenyl derivatives of borane - Valuable reagents for the isoprenylboration of aldehydes. A convenient route to both enantiomers of ipsenol and ipsdienol in high optical purity

Doi:10.1016/S0040-4020(01)85575-7
(1990)

Article Doi