Two Cu(Ⅱ) complexes with title Schiff base ligand H 2L, micro crystal Cu(HL)ClO 4·H 2O and single crystal , have been synthesized and characterized by IR spectra, etc .. By cyclic voltammetry, a quasi reversible...Two Cu(Ⅱ) complexes with title Schiff base ligand H 2L, micro crystal Cu(HL)ClO 4·H 2O and single crystal , have been synthesized and characterized by IR spectra, etc .. By cyclic voltammetry, a quasi reversible electron transferring process has been shown in Cu(Ⅱ)/Cu(Ⅰ) couples reaction of ; the given value E 0 1/2 =-0.73 V has been estimated. The structure of has been determined by X ray diffraction with R =0.036. The results indicate that the deprotonic ligand, as a practically tetradentate, coordinates only with its two imino and two phenoxo groups to form a D 2d symmetric geometry. Two different torsional modes of the homologous ligands, occurring in mono and di nuclear Cu(Ⅱ) complexes, respectively, have been contrasted and discussed.展开更多
Reaction of 2,4-di-Eert-butyl-phenol,ethylenediamine and formaldehyde （37% solution in water）in 2:1:5molar ratio in methanol afforded the 1,2-bis[3-（6,8-di-tert-butyl-3,4-dihydro-2[H]-1,3-benzoxazine）-yl]ethane in...Reaction of 2,4-di-Eert-butyl-phenol,ethylenediamine and formaldehyde （37% solution in water）in 2:1:5molar ratio in methanol afforded the 1,2-bis[3-（6,8-di-tert-butyl-3,4-dihydro-2[H]-1,3-benzoxazine）-yl]ethane in high yields.This compound was fully characterized by elemental analysis,1H NMR,MS,and IR spectroscopies.The crystal structure of the title compound was determined by X-ray diffraction method.It crystallizes in triclinic,space group P（1）,a=0.5727（2）,b=0.9268（3）,c=1.4666（4）nm,a=88.12（1）°,β=88.54（1）°,γ=80.82（1）°,V=0.7679（4）nm3,Z=1,DC=1.126Mg·m-3,F（000）=286,μ（MoKα）=0.69cm-1,R=0.048,wR=0.140.This compound had a centrosymmetrical structure.展开更多
R ) and ( S ) (2 benzyloxyethyl)oxirane 1 were prepared from ( S ) and ( R ) aspartic acid by modification of the procedure described by Rapoport. Aspartic acid was converted into bromosuccinic acid 2 by treatment wit...R ) and ( S ) (2 benzyloxyethyl)oxirane 1 were prepared from ( S ) and ( R ) aspartic acid by modification of the procedure described by Rapoport. Aspartic acid was converted into bromosuccinic acid 2 by treatment with sodium nitrite/potassium bromide/sulfuric acid,the diacid 2 was then reduced with freshly prepared boron trifluoride ethyl ether complex to bromodiol 3, which was further treated with sodium hydride and benzylbromide/TBAI(tetrabutylammonium iodide) to afford (2 benzyloxyethyl)oxirane. This procedure has shown the good yield, mild condition and excellent enantiomeric purity of the product.展开更多
文摘Two Cu(Ⅱ) complexes with title Schiff base ligand H 2L, micro crystal Cu(HL)ClO 4·H 2O and single crystal , have been synthesized and characterized by IR spectra, etc .. By cyclic voltammetry, a quasi reversible electron transferring process has been shown in Cu(Ⅱ)/Cu(Ⅰ) couples reaction of ; the given value E 0 1/2 =-0.73 V has been estimated. The structure of has been determined by X ray diffraction with R =0.036. The results indicate that the deprotonic ligand, as a practically tetradentate, coordinates only with its two imino and two phenoxo groups to form a D 2d symmetric geometry. Two different torsional modes of the homologous ligands, occurring in mono and di nuclear Cu(Ⅱ) complexes, respectively, have been contrasted and discussed.
文摘Reaction of 2,4-di-Eert-butyl-phenol,ethylenediamine and formaldehyde （37% solution in water）in 2:1:5molar ratio in methanol afforded the 1,2-bis[3-（6,8-di-tert-butyl-3,4-dihydro-2[H]-1,3-benzoxazine）-yl]ethane in high yields.This compound was fully characterized by elemental analysis,1H NMR,MS,and IR spectroscopies.The crystal structure of the title compound was determined by X-ray diffraction method.It crystallizes in triclinic,space group P（1）,a=0.5727（2）,b=0.9268（3）,c=1.4666（4）nm,a=88.12（1）°,β=88.54（1）°,γ=80.82（1）°,V=0.7679（4）nm3,Z=1,DC=1.126Mg·m-3,F（000）=286,μ（MoKα）=0.69cm-1,R=0.048,wR=0.140.This compound had a centrosymmetrical structure.
文摘R ) and ( S ) (2 benzyloxyethyl)oxirane 1 were prepared from ( S ) and ( R ) aspartic acid by modification of the procedure described by Rapoport. Aspartic acid was converted into bromosuccinic acid 2 by treatment with sodium nitrite/potassium bromide/sulfuric acid,the diacid 2 was then reduced with freshly prepared boron trifluoride ethyl ether complex to bromodiol 3, which was further treated with sodium hydride and benzylbromide/TBAI(tetrabutylammonium iodide) to afford (2 benzyloxyethyl)oxirane. This procedure has shown the good yield, mild condition and excellent enantiomeric purity of the product.
