Dong-Bin Dang

Assembly of polyoxometalate-based inorganic–organic compounds from silver–Schiff base building blocks: synthesis, crystal structures and luminescent properties

Three polyoxometalate-based inorganic–organic hybrid compounds constructed from silver(I)-L (L = N,N′-bis-pyridin-2-ylmethylene-hydrazine) species and saturated Keggin type polyoxoanions, {[Ag3L3](PW12O40)(CH3CN)(DMF)2.5}n (1), [Ag4L3(CH3CN)4][Ag2L(CH3CN)3](PMo12O40)2·CH3CN (2) and [(SiMo12O40){Ag2L(CH3CN)3}2]·(CH3CN)2 (3), have been synthesized and structurally characterized by IR spectroscopy, UV spectroscopy, thermogravimetric (TG) analyses and complete single crystal structure analyses. The structure of 1 containing [PW12O40]3− anions as templates exhibits a one-dimensional chain structure constructed by the coordination of a silver center and bis-bidentate bridging ligands with the pyridyl rings adopting a transoid configuration. Compound 2 displays an AB-type arrangement supramolecular structure, in which A is a two-dimensional sheet formed by linking the adjacent [Ag4L3(CH3CN)4]4+ units through the cooperativity of intermolecular π–π interactions and C–H⋯π interactions, while B is composed of [PMo12O40]3− anions and binuclear [Ag2L(CH3CN)4]2+ cations. Compound 3 exhibits a new bisupporting Keggin-polyoxometalate structure in which the [SiMo12O40]4− core supports two [Ag2L(CH3CN)3]2+ fragments in two opposite positions. The luminescent properties of L and 1–3 in the solid state were investigated.

Three-dimensional homochiral manganese–lanthanide frameworks based on chiral camphorates with multi-coordination modes

A series of 3D homochiral manganese-lanthanide frameworks have been synthesized based on chiral camphoric acid. In the heterometallic features, D-camphoric acids are unprecedentedly embedded in three coordination modes.

A series of metal–organic frameworks based on polydentate Schiff-base ligands derived from benzil dihydrazone: synthesis, crystal structures and luminescent properties

A series of metal–organic frameworks {[AgL1]ClO4}n (1), {[AgL12]BF4}n (2), {[AgL1(NO3)](CH3CH2OH)}n (3), {[ZnL12(NCS)2]CH3CN}n (4), [AgL2(NO3)]n (5), {[FeL22Cl2]·CH3CN}n (6), {[MnL22(NCS)2]·(CH3CH2OH)}n (7) and [ZnL22(NCS)2]n (8) have been synthesized and structurally characterized by IR spectroscopy, UV spectroscopy, thermogravimetric (TG) analyses, luminescent spectroscopy and complete single-crystal structure analyses, where L1 is (N′,N′-bis[1-(pyridin-4-yl)methylidene]benzil dihydrazone) and L2 is (N′,N′-bis[1-(pyridin-3-yl)methylidene]benzil dihydrazone), respectively. The structure of 1 exhibits a two-dimensional layer network featuring trimetal 36-membered non-planar macrocycles. Polymer 2 is a one-dimensional chain structure with tetranuclear metallacyclic rings. For polymer 3, each ligand acts as a bidentate ligand to bind two Ag(I) centers and each silver center is coordinated to two N-donors from two ligands forming a one-dimensional chain. Polymer 4 displays a two-dimensional layer network containing tetranuclear 68-membered metallocyclic rings. Polymers [AgL2(NO3)]n (5), {[FeL22Cl2]·CH3CN}n (6), {[MnL22(NCS)2]·(CH3CH2OH)}n (7) and [ZnL22(NCS)2]n (8) show all one-dimensional chain structures containing bimetallic 8-membered rings and tetrametallic 42-membered rings for 5, bimetallic 34-membered quadrangular rings for 6 and 7, and bimetallic 30-membered quadrangular rings for 8, respectively. The luminescent properties of L1, L2 and 1–8 in the solid state were investigated.

Assembly of four d10-metal inorganic–organic hybrid coordination polymers based on bipyrazine imine-based ligand: Synthesis, crystal structures and luminescent properties

Four new inorganic–organic hybrid coordination polymers {[Ag2L(NO3)2]·H2O}n (1), [Ag2L(SCN)2]n (2), [CdL(SCN)2]n (3), and [CdLI2]n (4) have been synthesized and structurally characterized by IR spectroscopy, thermogravimetric (TG) analyses and complete single crystal structure analyses, where L is 2,5-bis(pyrazinyl)-3,4-diaza-2,4-hexadiene. The structure of polymer 1 is a 3D coordination framework containing Ag-(μ-NO3−) inorganic bridging units, in which each L coordinates four silver atoms through two pyrazinylimine chelate units and two terminal monodentate pyrazinyl N donors. Polymer 2 displays a new 3D inorganic–organic hybrid network through the coordination interactions between Ag-(1,1,3-μ-SCN−) inorganic 2D sheets and bidentate bridging ligands with two terminal monodentate pyrazinyl N donors. Bidentate bridging ligands link 1D inorganic chains Cd-(1,3-μ-SCN−) system for 3 and Cd-(μ-I−) system for 4 to form a similar two-dimensional layer network. The luminescent properties of polymers 1–4 were investigated in the solid state at room temperature.

Two copper(II) complexes with 4-benzoylpyridine ligand: synthesis, crystal structure and luminescent properties.

Two new copper(II) complexes Cu(NCS)2(4-Bzpy)2 (1) and Cu(NO3)2(4-Bzpy)4 (2) (4-Bzpy=4-benzoylpyridine) have been synthesized and characterized by IR, UV, elemental analysis and X-ray crystallography. Cu(II) atom has a square planar environment for 1 and an distorted octahedral environment for 2, respectively. In solid state there are C-H⋯π interactions and C-H⋯S hydrogen bonds between adjacent molecules in complex 1. The molecule of complex 2 is further connected by multiform π-π interactions, C-H⋯π interactions and C-H⋯O hydrogen bonds to form a three-dimensional supramolecular structure. The luminescent properties of the complexes 1 and 2 were both investigated in H2O solution and in solid state at room temperature, respectively.

Two one-dimension copper(II) coordination polymers based on imine-based bidentate Schiff-base ligand: synthesis, crystal structure and luminescent properties.

Two new one-dimension copper(II) coordination polymers [CuL(2)(NCS)(2)](n) (1) and [CuL(2)(NO(3))(2)](n) (2) (L=(C(5)H(4)N)C(CH(3))=N-N=(CH(3))C(C(5)H(4)N)) have been synthesized and characterized by IR, elemental analysis, TG technique and X-ray crystallography. Each Cu(II) atom has a distorted octahedral N(6) (1) or N(4)O(2) (2) environment with four pyridyl N atoms from four ligands and two N atoms from two NCS(-) anions for polymer 1 or two O atoms from two NO(3)(-) anions for polymer 2, respectively. A pair of bis-monodentate bridging ligands links two Cu(II) centers to form one dimension chain structure containing bimetallic 22-membered macrometallacyclic rings. 1D chain is held together with its neighboring ones via C-H⋯S hydrogen bonds for 1 and C-H⋯O hydrogen bonds, C-H⋯π interactions for 2 to form a 3D supramolecular structure, respectively. The luminescent properties of the polymers 1 and 2 were investigated in the solid state at room temperature.

A one-dimensional polyoxometalate-based polymer [Cu(DMF)6][PMoVMoVI11O40Cu(DMF)4]·DMF: Crystal structure and luminescent properties

The polyoxometalate-based 1D coordination polymer [[Cu(DMF)₆][PMo(V)Mo(VI)₁₁O₄₀Cu(DMF)₄]·DMF1 was synthesized and characterized by IR, UV spectroscopy and single-crystal X-ray diffraction analysis. Each Cu(II) center has a distorted octahedral coordination geometry. Cu(1) center interconnects with two [PMo(V)Mo(VI)₁₁O₄₀]⁴⁻ anion subunits and each [PMo(V)Mo(VI)(11)O(40)]⁴⁻ polyoxoanion acts as a didentate ligand to link two Cu centers through two terminal oxygen atoms to form a one-dimensional chain structure. The luminescent properties of 1 in the solution and in the solid state were investigated, respectively.

Synthesis, Crystal Structure, and Luminescent Properties of One Cadmium(II) Coordination Polymer with Mixed Imine-based Bidentate Schiff-Base and Thiocyanate Ligands

A new one-dimension Cd(II) coordination polymer [CdL2(NCS)2] n (L = (C5H4N)C(CH3) = N−N = C(CH3)(C5H4N)) has been synthesized and characterized by IR, UV, elemental analysis, TG technique and X-ray crystallography. Cd(II) atom has an distorted octahedral environment with a N6 donor set from four ligands and two NCS− anions, respectively. A pair of ligands bridge two adjacent Cd(II) centers to form one dimension chain structure containing bimetallic 22-membered macrometallacyclic rings. A 1D structure is held together with its neighboring ones via multiform hydrogen bonds to form a 3D supramolecular structure. The luminescent properties of the complex at room temperature were investigated.

Preparation, characterization and crystal structure of an intermolecular compound based on H3PMo12O40·nH2O and diethylamine

AbstractAn intermolecular compound, H3PMo12O40·5(CH3CH2)2NH·H2O, between the heteropolymolybdate α-H3PMo12O40 and the organic substrate diethylamine, has been synthesized and characterized. Light yellow crystals of the title compound were crystallized from a mixed solvent of water and acetonitrile with formula H3PMo12O40·5(CH3CH2)2NH·H2O. Spectroscopic data support the presence of a sizable electronic interaction between the organic substrate and the inorganic anion in the solid state. The single crystal x-ray structure analysis of the title compound revealed that it crystallized in the triclinic system, space group P