87361-23-7Relevant articles and documents
Selective P?C(sp3) Bond Cleavage and Radical Alkynylation of α-Phosphorus Alcohols by Photoredox Catalysis
Jia, Kunfang,Li, Junzhao,Chen, Yiyun
, p. 3174 - 3177 (2018/02/09)
Herein the first P?C(sp3) bond cleavage and radical alkynylation of α-phosphorus alcohols to construct phosphonoalkynes is reported. The phosphorus radical is generated upon P?C bond cleavage reaction via the alkoxyl radical through photoredox catalysis with cyclic iodine(III) reagents. Various arylphosphinoyl-, alkylphosphinoyl-, phosphonate-, and phosphonic amide alcohols serve as radical phosphorus precursors to construct phosphonoalkynes for the first time.
Push-pull acylo-phosphine oxides for two-photon-induced polymerization
Nazir, Rashid,Danilevicius, Paulius,Gray, David,Farsari, Maria,Gryko, Daniel T.
, p. 7239 - 7244 (2013/10/21)
The two-step method for the synthesis of acyl-phosphine oxides from aromatic aldehydes was optimized giving the products in 52-97% overall yield. Linear and nonlinear optical properties of series of acyl-phosphine oxides possessing substituents with different electron-donating ability were investigated. Two-photon absorption cross sections (σ2) of push-pull acyl-phosphine oxide was determined as 9GM via z-scan measurements with femtosecond laser pulses. Using acyl-phosphine oxides possessing dipolar structure as initiators, 3D nanopatterns were successfully fabricated by two-photon initiated polymerization. These compounds also initiate classical photopolymerization when excited with UV radiation.
Investigations about the Electronic Influences on the Reactivity of Aroyl- and Acyldiphenylphosphanes and their Resulting Products
Lindner, Ekkehard,Huebner, Dieter
, p. 2574 - 2590 (2007/10/02)
The air sensitive aroyl- and acyldiphenylphosphanes RC(O)-PPh2 (2a - i) are obtained by reaction of the acyl chlorides RC(O)Cl (1a - i) with (CH3)3Si-PPh2 in petroleum ether.On access of water 2a - i are hydrolysed immediately.Starting from η5-C5H5Mn(CO)2THF (3x), BrMn(CO)5 (3y) and 2c - f the stable complexes LnMn-PPh2-C(O)R (4cx,dx,ey,fx) are formed. 1b - d, f - i can be transformed into the phosphane oxides RC(O)-P(O)Ph2 (5b - d, f - i) by Arbusov reaction with Ph2POCH3.From the oxides 5b - d, f and water, by a one pot reaction of 2b - d, f with HP(O)Ph2 andoxygen, or by the action of HP(O)Ph2 on 5a, f, the phosphinates -CHR (6a - d, f) are formed. 6a is produced also in form of the picolinium chloride 6a'.The electronic influences of the different aroyl residues on the reactivity of the aroylphosphanes 2c, d, f are investigated on the basis of the electronic and i.r. spectra of 4cx, dx, fx.The unusual stability of the methoxy compound 5f can be traced back to the strong +M effect of the 4-methoxybenzoyl residue.