Reactions of CdX2(X=NO3-, ClO4-) with Hatza (atza=5-aminotetrazole-1-acetato anion) and 2,2′-bipyridine (2,2′-bipy) or 1,10-phenanthroline (1,10-phen) in a methanol/aqueous solution produced a set of new Cd...Reactions of CdX2(X=NO3-, ClO4-) with Hatza (atza=5-aminotetrazole-1-acetato anion) and 2,2′-bipyridine (2,2′-bipy) or 1,10-phenanthroline (1,10-phen) in a methanol/aqueous solution produced a set of new Cd(Ⅱ) coordination polymers, {[Cd(atza)(H2O)(2,2′-bipy)]ClO4}n (1), {[Cd(atza)(H2O)(1,10-phen)]ClO4 }n (2), {[Cd(atza)(H2O)(2,2′-bipy)]NO3}n (3) and {[Cd(atza)2 (1,10-phen)]·0.5H2O}n (4). Single-crystal X-ray diffraction analysis reveals that each Cd(Ⅱ) ion has a distorted octahedral coordination geometry in 1-4, and the Cd(Ⅱ) ion centers are connected through the tridentate atza bridging ligands to form a 2D layer (1-3) or ID chain (4) structure. The fluorescent properties of 2 and 4 are also discussed.展开更多
Two new tetrazole 1-acetato complexes, [Ag(1-tza)(phen)]∞ (1) and [Cd(1- tza)2(2,2'-bipy)]∞ (2) (1-Htza = tetrazole 1-acetato, phen = 1,10-phenanthroline, 2,2'-bipy = 2,2'-bipyridine), have been syn...Two new tetrazole 1-acetato complexes, [Ag(1-tza)(phen)]∞ (1) and [Cd(1- tza)2(2,2'-bipy)]∞ (2) (1-Htza = tetrazole 1-acetato, phen = 1,10-phenanthroline, 2,2'-bipy = 2,2'-bipyridine), have been synthesized by solvothermal synthesis and structurally characterized by elemental analyses, IR spectra and single-crystal X-ray diffraction. Complex 1 shows a 1-D chained structure, while the structure of 2 contains two 1-D chains, which is the first 1-tza-based complex containing three different coordination modes of the 1-tza ligand. The aromatic stacking effects play an important role in the formation of supramolecular frameworks of these two complexes. Photoluminescent studies show that the two complexes exhibit efficient luminescence. In addition, optical diffuse reflectance spectra and thermogravimetric analyses of 1 and 2 have also been investigated.展开更多
The crystal of the title complex with formula C48H52N8O16CI2Cd3(Mr=1405. 10) was crystallized in monoclinic, space group P21/n, with a=12. 666 (3), b=18. 306(6), c=13. 231 (4) A, p=111. 68(3), V=2851 (2) A3, Z=2, Dr=1...The crystal of the title complex with formula C48H52N8O16CI2Cd3(Mr=1405. 10) was crystallized in monoclinic, space group P21/n, with a=12. 666 (3), b=18. 306(6), c=13. 231 (4) A, p=111. 68(3), V=2851 (2) A3, Z=2, Dr=1. 637 g/cm-3 p=12. 680 cm-1, F(000)=1404. The final refinement is convergedwith R=0. 052 and Rw=0. 055. In the molecule [Cd3(py8(Oac)4] (CIO4)2, the aver-age values of Cd-N and Cd-O bonds are 2. 306 and 2. 288 A, respectively. In thecanon of the title complex. each Cd atom is coordinated by N and O atoms, which arefrom pyridine molecules and acetatoes, respectively, to form a distorted octahedron.And three Cd atoms are linked by two u2-O atoms of two acetatoes and other two u-ac-etato side bridges.展开更多
The crystal structure of the title compound {[Mn(phen)2(OAc)(H2O)]ClO4}2H2O (phen = 1,10-phenanthroline) has been synthesized and determined by X-ray diffraction. The crystal is of triclinic, space group P?with a = 12...The crystal structure of the title compound {[Mn(phen)2(OAc)(H2O)]ClO4}2H2O (phen = 1,10-phenanthroline) has been synthesized and determined by X-ray diffraction. The crystal is of triclinic, space group P?with a = 12.7955(4), b = 15.0544(4), c = 16.2183(4) , ?= 64.479(1), b =67.526(1), g = 83.582(1), C52H40Cl2Mn2N8O15, Mr = 1197.70, V = 2600.1(1) ?, Dc = 1.530 g/cm3, F(000) = 1224, = 0.666 cm-1 and Z = 2. The final refinement gave R = 0.0691 and wR = 0.1821 for 6131 observed reflections with I > 2s(I). The cell of the complex contains two uniform mono-manganese molecules [Mn(phen)2(OAc)(H2O)]ClO4 and a solvate water molecule. Four nitrogen atoms from two chelating phenanthroline ligands and one oxygen atom from acetate ligate to the MnⅡ ion, forming a distorted octahedral geometry together with one coordinated water molecule. One ClO4- anion and one water molecule exist outside the cation [Mn(phen)2(OAc)- (H2O)]+ as a counter ion and solvate molecule, respectively.展开更多
基金supported by the Foundation of Suzhou Science and Technology of Jiangsu Province(SYN201015)Key Laboratory of Advanced Functional Materials of Jiangsu Province of China (No.10KFJJ002)
文摘Reactions of CdX2(X=NO3-, ClO4-) with Hatza (atza=5-aminotetrazole-1-acetato anion) and 2,2′-bipyridine (2,2′-bipy) or 1,10-phenanthroline (1,10-phen) in a methanol/aqueous solution produced a set of new Cd(Ⅱ) coordination polymers, {[Cd(atza)(H2O)(2,2′-bipy)]ClO4}n (1), {[Cd(atza)(H2O)(1,10-phen)]ClO4 }n (2), {[Cd(atza)(H2O)(2,2′-bipy)]NO3}n (3) and {[Cd(atza)2 (1,10-phen)]·0.5H2O}n (4). Single-crystal X-ray diffraction analysis reveals that each Cd(Ⅱ) ion has a distorted octahedral coordination geometry in 1-4, and the Cd(Ⅱ) ion centers are connected through the tridentate atza bridging ligands to form a 2D layer (1-3) or ID chain (4) structure. The fluorescent properties of 2 and 4 are also discussed.
基金supported by the NSF of Jiangxi Province(51302041)the Fujian Institute of Research on the Structure of Matter(20140014)the Key Laboratory of University for Materials Chemistry
文摘Two new tetrazole 1-acetato complexes, [Ag(1-tza)(phen)]∞ (1) and [Cd(1- tza)2(2,2'-bipy)]∞ (2) (1-Htza = tetrazole 1-acetato, phen = 1,10-phenanthroline, 2,2'-bipy = 2,2'-bipyridine), have been synthesized by solvothermal synthesis and structurally characterized by elemental analyses, IR spectra and single-crystal X-ray diffraction. Complex 1 shows a 1-D chained structure, while the structure of 2 contains two 1-D chains, which is the first 1-tza-based complex containing three different coordination modes of the 1-tza ligand. The aromatic stacking effects play an important role in the formation of supramolecular frameworks of these two complexes. Photoluminescent studies show that the two complexes exhibit efficient luminescence. In addition, optical diffuse reflectance spectra and thermogravimetric analyses of 1 and 2 have also been investigated.
文摘The crystal of the title complex with formula C48H52N8O16CI2Cd3(Mr=1405. 10) was crystallized in monoclinic, space group P21/n, with a=12. 666 (3), b=18. 306(6), c=13. 231 (4) A, p=111. 68(3), V=2851 (2) A3, Z=2, Dr=1. 637 g/cm-3 p=12. 680 cm-1, F(000)=1404. The final refinement is convergedwith R=0. 052 and Rw=0. 055. In the molecule [Cd3(py8(Oac)4] (CIO4)2, the aver-age values of Cd-N and Cd-O bonds are 2. 306 and 2. 288 A, respectively. In thecanon of the title complex. each Cd atom is coordinated by N and O atoms, which arefrom pyridine molecules and acetatoes, respectively, to form a distorted octahedron.And three Cd atoms are linked by two u2-O atoms of two acetatoes and other two u-ac-etato side bridges.
基金This work was supported by the State Key Basic Research and Development Plan (G1998010100) and NNSFC (No. 30170229 29973047 and 39970177)
文摘The crystal structure of the title compound {[Mn(phen)2(OAc)(H2O)]ClO4}2H2O (phen = 1,10-phenanthroline) has been synthesized and determined by X-ray diffraction. The crystal is of triclinic, space group P?with a = 12.7955(4), b = 15.0544(4), c = 16.2183(4) , ?= 64.479(1), b =67.526(1), g = 83.582(1), C52H40Cl2Mn2N8O15, Mr = 1197.70, V = 2600.1(1) ?, Dc = 1.530 g/cm3, F(000) = 1224, = 0.666 cm-1 and Z = 2. The final refinement gave R = 0.0691 and wR = 0.1821 for 6131 observed reflections with I > 2s(I). The cell of the complex contains two uniform mono-manganese molecules [Mn(phen)2(OAc)(H2O)]ClO4 and a solvate water molecule. Four nitrogen atoms from two chelating phenanthroline ligands and one oxygen atom from acetate ligate to the MnⅡ ion, forming a distorted octahedral geometry together with one coordinated water molecule. One ClO4- anion and one water molecule exist outside the cation [Mn(phen)2(OAc)- (H2O)]+ as a counter ion and solvate molecule, respectively.