40743-08-6Relevant articles and documents
Persistent room temperature blue phosphorescence from racemic crystals of 1,1-diphenylmethanol derivatives
Ishigaki, Kaname,Karatsu, Takashi,Taniguchi, Tatsuo,Yamada, Masaru
, (2021)
Among the six alkyldiphenylmethanol derivatives assessed in this study, five showed persistent room temperature phosphorescence (pRTP), whereas the original diphenylmethanol (DPhHOH) did not. pRTP is a unique luminescence phenomenon that appears only in t
Synthesis of N,N-dimethylaminopyrene-modified short peptides for chemical photocatalysis
Hermann, Sergej,Wagenknecht, Hans-Achim
, p. 563 - 566 (2017)
The synthesis of peptide-based photocatalysts that use 1-N,N-dimethylaminopyrene as chromophore and their application in photocatalysis is reported. The copper(I)-catalyzed alkyne-azide cycloaddition was applied as key step to prepare the peptide–pyrene c
Iron-catalyzed π-activated C-O ether bond cleavage with C-C and C-H bond formation
Fan, Xiaohui,Cui, Xiao-Meng,Guan, Yong-Hong,Fu, Lin-An,Lv, Hao,Guo, Kun,Zhu, Hong-Bo
supporting information, p. 498 - 501 (2014/02/14)
A novel and efficient allylic alkylation reaction between π-activated ethers and allylsilane was realized under mild conditions through iron(III)-catalyzed C sp 3-O ether bond cleavage. The present protocol provides an attractive approach for the construction of sp3-sp3 C-C bonds and can be potentially applied for the selective reduction of benzyl and allyl ethers to their corresponding hydrocarbon compounds by using triethylsilane as a hydride-transfer reagent. A mild, economical, and environmentally friendly method for the construction of C sp 3-C sp 3 bonds through iron-catalyzed π-activated C-O ether bond cleavage is developed. In addition, this catalytic system can be used for the selective reduction of benzylic and allylic C-O ether bonds to C-H bonds. Copyright
