A novel Schiff base ligand (HL) derived from S-methyldithiocabazate and pmethoxylbenzaldehyde was prepared and characterized. The Schiff base ligand acts as a single negatively charged bidentate ligand fondng D-M-D ty...A novel Schiff base ligand (HL) derived from S-methyldithiocabazate and pmethoxylbenzaldehyde was prepared and characterized. The Schiff base ligand acts as a single negatively charged bidentate ligand fondng D-M-D type comPlex (D=donor, M=metal). Single crystal X-ray diffraction analysis of the copper(Ⅱ) complex established that the geometry around Cu (Ⅱ) is square-planar with two equivalent M-N and M-S bonds. The two phenyl rings and the coordinated plane are almost in one plane fotheng an electronic delocalization system. Their thirdorder response was also studied.展开更多
The self-assembly of a prominent mixed-donor ligand, 5-[4-（1H-tetrazolyl）phen]isophthalic acid（H3TZPl）, with a Cd2＋ center generates two new metal-organic frameworks： [Cd（H2TZPI）2（H2O）2]n（JUC-163） and [Cd2...The self-assembly of a prominent mixed-donor ligand, 5-[4-（1H-tetrazolyl）phen]isophthalic acid（H3TZPl）, with a Cd2＋ center generates two new metal-organic frameworks： [Cd（H2TZPI）2（H2O）2]n（JUC-163） and [Cd2（TZPI）（μ3-OH）（H2O）2]-H2O.DMF（JUC-164）. The two complexes demonstrate different structures for the ligand＇s different coordination modes and configurations. JUC-163 shows a 2D layer structure and further forms into a 3D supramolecular framework by noncovalent interactions（C--H…O, O--H…N and π…π interactions）, whereas JUC-164 exhibits a fascinating 3D framework for the outstanding coordination modes and configurations of the ligand, which are fit for the complex structure. And also, the factor of different cadmium salts（chloride and nitrate） which are used in synthesis progress is worth to notice for the construction of the two distinct structures. The luminescent properties of these metal-organic frameworks were also investigated.展开更多
Chiral S,P-donor ferrocene-derived ligands were synthesized and applied in the asymmetric hydrogenation of quinolines using the [Ir(COD)Cl]2/S,P-ligand c omplex a s the catalyst in the presence of iodine. The effects ...Chiral S,P-donor ferrocene-derived ligands were synthesized and applied in the asymmetric hydrogenation of quinolines using the [Ir(COD)Cl]2/S,P-ligand c omplex a s the catalyst in the presence of iodine. The effects of the solvent and hydroge n pressure on conversion and enantioselectivity were examined, and up to 82% ee was obtained. The planar chirality plays an important role in this reaction. R- and S-enantiomers of 1,2,3,4-tetrahydroquinoline derivatives were ob tained using ligands 3 and 5, respectively.展开更多
A new metal-organic framework based on bbi and PHBA（bbi = 1,1＇-（1, 4-butanediyl）bis（imidazole）, PHBA = p-hydroxybenzoic acid）, namely, [Cd（bbi）（PHBA）2]n（1） has been synthesized by the conventional method....A new metal-organic framework based on bbi and PHBA（bbi = 1,1＇-（1, 4-butanediyl）bis（imidazole）, PHBA = p-hydroxybenzoic acid）, namely, [Cd（bbi）（PHBA）2]n（1） has been synthesized by the conventional method. Compound 1 displays a two-dimensional（2D） layer structure possessing the left-and right-handed helical chains and stabilized by intermolecular hydrogen-bonding to form a three-dimensional（3D） supramolecular structure. Topologically, the 2D layer belongs to well-known（4,4） network topology. The structure has been determined by single-crystal X-ray diffraction analyses, and further characterized by infrared spectra（IR）, elemental analyses and powder X-ray diffraction. In addition, the thermal behavior and luminescent properties of [Cd（bbi）（PHBA）2]n have been investigated in detail.展开更多
A novel complex of monomeric thallium(III) with the nitrogen donor ligand phenanthroline (phen) has been prepared and characterized by multinuclear NMR (1H, 13C, 205Tl). The three complexes exist in equilibria in DMSO...A novel complex of monomeric thallium(III) with the nitrogen donor ligand phenanthroline (phen) has been prepared and characterized by multinuclear NMR (1H, 13C, 205Tl). The three complexes exist in equilibria in DMSO and acetonitrile solution, which was proved by the 205Tl NMR spectra. The 1H and 13C NMR spectra of tris-phen Tl(III) complex have been measured, where the spin-spin coupling between Tl (I = 1/2) and 13C or 1H signals were observed with the 1H and 13C NMR spectroscopy in acetonitrile. The coupling constants are presented and the chemical shifts of complexes are discussed in detail.展开更多
文摘A novel Schiff base ligand (HL) derived from S-methyldithiocabazate and pmethoxylbenzaldehyde was prepared and characterized. The Schiff base ligand acts as a single negatively charged bidentate ligand fondng D-M-D type comPlex (D=donor, M=metal). Single crystal X-ray diffraction analysis of the copper(Ⅱ) complex established that the geometry around Cu (Ⅱ) is square-planar with two equivalent M-N and M-S bonds. The two phenyl rings and the coordinated plane are almost in one plane fotheng an electronic delocalization system. Their thirdorder response was also studied.
文摘The self-assembly of a prominent mixed-donor ligand, 5-[4-（1H-tetrazolyl）phen]isophthalic acid（H3TZPl）, with a Cd2＋ center generates two new metal-organic frameworks： [Cd（H2TZPI）2（H2O）2]n（JUC-163） and [Cd2（TZPI）（μ3-OH）（H2O）2]-H2O.DMF（JUC-164）. The two complexes demonstrate different structures for the ligand＇s different coordination modes and configurations. JUC-163 shows a 2D layer structure and further forms into a 3D supramolecular framework by noncovalent interactions（C--H…O, O--H…N and π…π interactions）, whereas JUC-164 exhibits a fascinating 3D framework for the outstanding coordination modes and configurations of the ligand, which are fit for the complex structure. And also, the factor of different cadmium salts（chloride and nitrate） which are used in synthesis progress is worth to notice for the construction of the two distinct structures. The luminescent properties of these metal-organic frameworks were also investigated.
文摘Chiral S,P-donor ferrocene-derived ligands were synthesized and applied in the asymmetric hydrogenation of quinolines using the [Ir(COD)Cl]2/S,P-ligand c omplex a s the catalyst in the presence of iodine. The effects of the solvent and hydroge n pressure on conversion and enantioselectivity were examined, and up to 82% ee was obtained. The planar chirality plays an important role in this reaction. R- and S-enantiomers of 1,2,3,4-tetrahydroquinoline derivatives were ob tained using ligands 3 and 5, respectively.
基金supported by the National Natural Science Foundation of China (Grant No.21968032)the Fundamental Research Funds of Central Universities-Innovation Team Cultivation Project (Grant No.31920190012)+1 种基金the Northwest Minzu University′s Double First-class and Characteristic Development Guide Special Funds-Chemistry Key Disciplines in Gansu Province (Grant No.11080316)the Teaching Quality and Reform Engineering Project of Gansu University (Grants No.2019GSSYJXSFZX01, 2019GSJXCGPY-16)
基金Supported by the Science and Technology Development Plan of Jilin Province(20150520006JH)Science and Technology Research Project of Education Department of Jilin Province(2016219)Science and Technology Development Plan of Siping City(2013055)
文摘A new metal-organic framework based on bbi and PHBA（bbi = 1,1＇-（1, 4-butanediyl）bis（imidazole）, PHBA = p-hydroxybenzoic acid）, namely, [Cd（bbi）（PHBA）2]n（1） has been synthesized by the conventional method. Compound 1 displays a two-dimensional（2D） layer structure possessing the left-and right-handed helical chains and stabilized by intermolecular hydrogen-bonding to form a three-dimensional（3D） supramolecular structure. Topologically, the 2D layer belongs to well-known（4,4） network topology. The structure has been determined by single-crystal X-ray diffraction analyses, and further characterized by infrared spectra（IR）, elemental analyses and powder X-ray diffraction. In addition, the thermal behavior and luminescent properties of [Cd（bbi）（PHBA）2]n have been investigated in detail.
基金The authors are grateful to the Swedish Natural Science Research Council (NFR) for financial support and together with the Knut and Alice Wallenberg foundation, for providing funds for purchasing the NMR spectrometersFinancial support of Overseas
文摘A novel complex of monomeric thallium(III) with the nitrogen donor ligand phenanthroline (phen) has been prepared and characterized by multinuclear NMR (1H, 13C, 205Tl). The three complexes exist in equilibria in DMSO and acetonitrile solution, which was proved by the 205Tl NMR spectra. The 1H and 13C NMR spectra of tris-phen Tl(III) complex have been measured, where the spin-spin coupling between Tl (I = 1/2) and 13C or 1H signals were observed with the 1H and 13C NMR spectroscopy in acetonitrile. The coupling constants are presented and the chemical shifts of complexes are discussed in detail.
