Yuan-Gen Yao
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Yuan-Gen Yao has a total of 26 co-authors. Here are the top co-authors by number of shared publications:
Zhao-Ji Li
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China
28 shared publicationsYao Kang
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China
27 shared publicationsYe-Yan Qin
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China
20 shared publicationsYi-Hang Wen
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, People's Republic of China
20 shared publicationsJian-Kai Cheng
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, People's Republic of China
19 shared publicationsJian Zhang
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, People's Republic of China
17 shared publications
Latest Publications
- 26 August 2010
- Published by Wiley in Chinese Journal of Chemistry
- Vol. 21 (9) , 1174-1177
P NMR studies on the ligand dissociation of trinuclear molybdenum cluster compounds
- 26 August 2010
- Published by Wiley in Chinese Journal of Chemistry
- Vol. 21 (9) , 1174-1177
P NMR studies on the ligand dissociation of trinuclear molybdenum cluster compounds
- 10 March 2007
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 63 (4) , m135-m136
Poly[μ2-trans-1,2-di-4-pyridylethylene-κ2N:N′-μ2-sulfato-κ2O:O′-zinc(II)]
The title compound, [Zn(SO(4))(C(12)H(10)N(2))](n), features a layered structure based on [Zn(SO(4))](n) spirals linked by 1,2-di-4-pyridylethylene (bpe) ligands, with the tetrahedral Zn and S atoms lying on twofold axes. The bpe ligands are centrosymmetric. The layers are linked by weak C-H...O interactions.
- 10 March 2007
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 63 (4) , m135-m136
Poly[μ2-trans-1,2-di-4-pyridylethylene-κ2N:N′-μ2-sulfato-κ2O:O′-zinc(II)]
The title compound, [Zn(SO(4))(C(12)H(10)N(2))](n), features a layered structure based on [Zn(SO(4))](n) spirals linked by 1,2-di-4-pyridylethylene (bpe) ligands, with the tetrahedral Zn and S atoms lying on twofold axes. The bpe ligands are centrosymmetric. The layers are linked by weak C-H...O interactions.
- 17 May 2006
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 2006 (11) , 2253-2258
Syntheses, Structures and Characterisation of Two CuII Polymers with 8‐Connected Topologies Based on Highly Connected SBUs
Two hydrothermally synthesised 3D metal‐coordination polymers, namely [Cu(isonicotinate)(nicotinate)]n (1), with an 8‐connected CsCl topology, and [Cu2(μ3‐OH)(isonicotinate)2(BDC)0.5]n (2), with an unusual 8‐connected 35.411.58.64 topology, demonstrate that highly connected SBUs can be employed in the construction of complicated frameworks. The temperature‐dependent magnetic susceptibilities for the two complexes were also determined. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
- 17 May 2006
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 2006 (11) , 2253-2258
Syntheses, Structures and Characterisation of Two CuII Polymers with 8‐Connected Topologies Based on Highly Connected SBUs
Two hydrothermally synthesised 3D metal‐coordination polymers, namely [Cu(isonicotinate)(nicotinate)]n (1), with an 8‐connected CsCl topology, and [Cu2(μ3‐OH)(isonicotinate)2(BDC)0.5]n (2), with an unusual 8‐connected 35.411.58.64 topology, demonstrate that highly connected SBUs can be employed in the construction of complicated frameworks. The temperature‐dependent magnetic susceptibilities for the two complexes were also determined. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
- 15 January 2005
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 61 (2) , m61-m63
Poly[[diaquacobalt(II)]-μ-4,4′-bipyridine-κ2N:N′-μ-p-phenylenebis(oxyacetato)-κ2O:O′]
The title compound, [CoII(C10H8O6)(C10H8N2)(H2O)2]n, was obtained by the hydrothermal reaction of CoSO(4) with benzene-1,4-dioxydiacetate [systematic name: p-phenylenebis(oxyacetate)] and 4,4'-bipyridine (4,4'-bpy). The Co atom lies at an inversion center and the benzene-1,4-dioxydiacetate and 4,4'-bipyridine moieties lie about other inversion centers. The benzene-1,4-dioxydiacetate ligands bridge the octahedral Co(II) coordination centers, forming a one-dimensional zigzag chain. The chains are further bridged by 4,4'-bpy ligands, forming a novel two-dimensional supramolecular architecture. Hydrogen-bonding interactions between the coordinated water molecules and the carboxylate O atoms lead to the formation of a three-dimensional network structure.
- 15 January 2005
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 61 (2) , m61-m63
Poly[[diaquacobalt(II)]-μ-4,4′-bipyridine-κ2N:N′-μ-p-phenylenebis(oxyacetato)-κ2O:O′]
The title compound, [CoII(C10H8O6)(C10H8N2)(H2O)2]n, was obtained by the hydrothermal reaction of CoSO(4) with benzene-1,4-dioxydiacetate [systematic name: p-phenylenebis(oxyacetate)] and 4,4'-bipyridine (4,4'-bpy). The Co atom lies at an inversion center and the benzene-1,4-dioxydiacetate and 4,4'-bipyridine moieties lie about other inversion centers. The benzene-1,4-dioxydiacetate ligands bridge the octahedral Co(II) coordination centers, forming a one-dimensional zigzag chain. The chains are further bridged by 4,4'-bpy ligands, forming a novel two-dimensional supramolecular architecture. Hydrogen-bonding interactions between the coordinated water molecules and the carboxylate O atoms lead to the formation of a three-dimensional network structure.
- 3 December 2004
- Published by Wiley in Zeitschrift für anorganische und allgemeine Chemie
- Vol. 630 (15) , 2731-2735
Syntheses and Crystal Structures of Two Metal Succinates Modified by Bipyridines
Two new metal succinates modified by rigid bipyridines, Cd(4, 4′‐bpy)(C4H4O4)·1/4H2O (1) and Cu(2, 2′‐bpy)(C4H4O4)0.5(NO3)(H2O) (2) (bpy = bipyridine), have been synthesized by hydrothermal reactions and structurally determined. Complex 1 crystallizes in the orthorhombic space group Cmca with the cell parameters a = 11.696(2), b = 15.554(2), c = 15.874(3) Å, α = β = γ = 90.00°, V = 2888(3) Å3, Z = 8. Complex 2 crystallizes in the triclinic space group $P{\bar 1}$ with a = 7.077(1), b = 9.838(2), c = 10.461(2) Å, α = 71.941(3)°, β = 73.078(3)°, γ = 74.502(3)°, V = 649.8(2) Å3, Z = 2. In complex 1, a 2‐D network was formed by Cd‐succinato bonding. The 2‐D networks are pillared by 4, 4′‐bpy ligands, forming a 3‐D grid framework. The 2‐fold interpenetration of the resulting 3‐D frameworks completes the molecular structure. In complex 2, the CuII atom adopts a distorted octahedral in which the CuII atoms are bridged by two H2O molecules into an infinite zigzag chain, [Cu2(H2O)2(C4H4O4)]n. The neighboring chains are further linked by π‐π stacking interactions into a 2‐D network, and the interlayer hydrogen bonds lead to the final 3‐D crystal structure.- 3 December 2004
- Published by Wiley in Zeitschrift für anorganische und allgemeine Chemie
- Vol. 630 (15) , 2731-2735
Syntheses and Crystal Structures of Two Metal Succinates Modified by Bipyridines
Two new metal succinates modified by rigid bipyridines, Cd(4, 4′‐bpy)(C4H4O4)·1/4H2O (1) and Cu(2, 2′‐bpy)(C4H4O4)0.5(NO3)(H2O) (2) (bpy = bipyridine), have been synthesized by hydrothermal reactions and structurally determined. Complex 1 crystallizes in the orthorhombic space group Cmca with the cell parameters a = 11.696(2), b = 15.554(2), c = 15.874(3) Å, α = β = γ = 90.00°, V = 2888(3) Å3, Z = 8. Complex 2 crystallizes in the triclinic space group $P{\bar 1}$ with a = 7.077(1), b = 9.838(2), c = 10.461(2) Å, α = 71.941(3)°, β = 73.078(3)°, γ = 74.502(3)°, V = 649.8(2) Å3, Z = 2. In complex 1, a 2‐D network was formed by Cd‐succinato bonding. The 2‐D networks are pillared by 4, 4′‐bpy ligands, forming a 3‐D grid framework. The 2‐fold interpenetration of the resulting 3‐D frameworks completes the molecular structure. In complex 2, the CuII atom adopts a distorted octahedral in which the CuII atoms are bridged by two H2O molecules into an infinite zigzag chain, [Cu2(H2O)2(C4H4O4)]n. The neighboring chains are further linked by π‐π stacking interactions into a 2‐D network, and the interlayer hydrogen bonds lead to the final 3‐D crystal structure.- 23 November 2004
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 60 (12) , m654-m656
Poly[[bis(pyridine-κN)copper(II)]-μ3-5-hydroxyisophthalato-κ3O:O′:O′′]
In the title compound, [Cu(C(8)H(4)O(5))(C(5)H(5)N)(2)](n) or [Cu(OH-BDC)(py)(2)](n) (where OH-H(2)BDC is 5-hydroxyisophthalic acid and py is pyridine), the Cu atoms are coordinated by two N atoms from the pyridine ligands and by three O atoms from hydroxyisophthalate ligands in a highly distorted triangular bipyramidal environment, with Cu-O distances in the range 1.941 (4)-2.225 (5) A and Cu-N distances of 2.014 (6) and 2.046 (6) A. The [Cu(OH-BDC)](n) two-dimensional network is built up from interlocking 22-, 15- and eight-membered rings via sharing of Cu atoms and O-H...O hydrogen bonds. Consolidation of the packing structure is achieved by edge- or point-to-face C-H...pi interactions and offset or slipped pi-pi stacking interactions.
- 23 November 2004
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 60 (12) , m654-m656
Poly[[bis(pyridine-κN)copper(II)]-μ3-5-hydroxyisophthalato-κ3O:O′:O′′]
In the title compound, [Cu(C(8)H(4)O(5))(C(5)H(5)N)(2)](n) or [Cu(OH-BDC)(py)(2)](n) (where OH-H(2)BDC is 5-hydroxyisophthalic acid and py is pyridine), the Cu atoms are coordinated by two N atoms from the pyridine ligands and by three O atoms from hydroxyisophthalate ligands in a highly distorted triangular bipyramidal environment, with Cu-O distances in the range 1.941 (4)-2.225 (5) A and Cu-N distances of 2.014 (6) and 2.046 (6) A. The [Cu(OH-BDC)](n) two-dimensional network is built up from interlocking 22-, 15- and eight-membered rings via sharing of Cu atoms and O-H...O hydrogen bonds. Consolidation of the packing structure is achieved by edge- or point-to-face C-H...pi interactions and offset or slipped pi-pi stacking interactions.
- 23 November 2004
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 60 (12) , m657-m658
Poly[aquaneodymium(III)-μ5-2-oxido-5-sulfonatobenzoato]
The title compound, [Nd(C(7)H(3)O(6)S)(H(2)O)](n) or [Nd(SSA)(H(2)O)](n) (H(3)SSA is 5-sulfosalicylic acid), was synthesized by the hydrothermal reaction of Nd(2)O(3) with H(3)SSA in water. The compound forms a three-dimensional network in which the asymmetric unit contains one Nd(III) atom, one SSA ligand and one coordinated water molecule. The central Nd(III) ion is eight-coordinate, bonded to seven O atoms from five different SSA ligands [Nd-O = 2.405 (4)-2.612 (4) angstroms] and one aqua O atom [Nd-OW = 2.441 (4) angstroms].
- 23 November 2004
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 60 (12) , m657-m658
Poly[aquaneodymium(III)-μ5-2-oxido-5-sulfonatobenzoato]
The title compound, [Nd(C(7)H(3)O(6)S)(H(2)O)](n) or [Nd(SSA)(H(2)O)](n) (H(3)SSA is 5-sulfosalicylic acid), was synthesized by the hydrothermal reaction of Nd(2)O(3) with H(3)SSA in water. The compound forms a three-dimensional network in which the asymmetric unit contains one Nd(III) atom, one SSA ligand and one coordinated water molecule. The central Nd(III) ion is eight-coordinate, bonded to seven O atoms from five different SSA ligands [Nd-O = 2.405 (4)-2.612 (4) angstroms] and one aqua O atom [Nd-OW = 2.441 (4) angstroms].
- 16 October 2004
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section E Structure Reports Online
- Vol. 60 (11) , o2029-o2031
4,4′-Bipyridylium bis(hydrogen 2,2′-dithiodibenzoate) dihydrate
- 16 October 2004
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section E Structure Reports Online
- Vol. 60 (11) , o2029-o2031
4,4′-Bipyridylium bis(hydrogen 2,2′-dithiodibenzoate) dihydrate
- 25 September 2004
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 60 (10) , m509-m511
Poly[[copper(II)-di-μ-5-aminoisophthalato(1–)-κ4 N:O] monohydrate]
The title compound, {[Cu(C8H6NO4)2]·H2O} n , was prepared by the hydrothermal assembly of 5-aminoisophthalic acid with copper nitrate. Single-crystal X-ray analysis shows that it has a two-dimensional layer coordination framework, in which the unique Cu atom lies on an inversion centre and adopts a square-planar geometry, coordinated to two N and two O atoms from symmetry-related ligands. The water molecule lies on a twofold axis and there are hydrogen-bonding interactions between the layers.
- 25 September 2004
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section C Crystal Structure Communications
- Vol. 60 (10) , m509-m511
Poly[[copper(II)-di-μ-5-aminoisophthalato(1–)-κ4 N:O] monohydrate]
The title compound, {[Cu(C8H6NO4)2]·H2O} n , was prepared by the hydrothermal assembly of 5-aminoisophthalic acid with copper nitrate. Single-crystal X-ray analysis shows that it has a two-dimensional layer coordination framework, in which the unique Cu atom lies on an inversion centre and adopts a square-planar geometry, coordinated to two N and two O atoms from symmetry-related ligands. The water molecule lies on a twofold axis and there are hydrogen-bonding interactions between the layers.
- 9 September 2004
- Published by Elsevier in Polyhedron
- Vol. 23 (14) , 2209-2215
Syntheses, structures and photoluminescent properties of 1D, 2D, 3D silver (I) coordination polymers with flexible long-chain dinitriles and tetranitriles
- 9 September 2004
- Published by Elsevier in Polyhedron
- Vol. 23 (14) , 2209-2215
Syntheses, structures and photoluminescent properties of 1D, 2D, 3D silver (I) coordination polymers with flexible long-chain dinitriles and tetranitriles