Unique Tetradentate Coordination of 2,2′-Bipyridyl-3,3′-Dicarboxylate (bpdc). Hydrothermal Synthesis and Crystal Structure of A Novel Polymeric Supramolecule [Co(bpdc)(H2O)2]n

2003 ◽  
Vol 56 (4) ◽  
pp. 335 ◽  
Author(s):  
Ben-Lai Wu ◽  
Hong-Quan Zhang ◽  
Hong-Yun Zhang ◽  
Qing-An Wu ◽  
Hong-Wei Hou ◽  
...  
Keyword(s):  
Title Complex ◽  
Water Molecules ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Pyridyl Nitrogen ◽  
Intermolecular Hydrogen Bonds ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
Polymeric Chains ◽  
Hydrothermal Methods

The title complex has been synthesized using hydrothermal methods and its structure determined by X-ray diffraction. It consists of polymeric chains of [Co(bpdc)(H2O)2] units (bpdc = 2,2′-bipyridyl-3,3′-dicarboxylate) which are linked by intermolecular hydrogen bonds to form two-dimensional layer-shaped supramolecules. Each bpdc ligand bridges two cobalt(II) centers in a rare tetradentate fashion through its two pyridyl nitrogen atoms chelating to one cobalt and two carboxyl oxygen atoms to the other in the equatorial plane. The octahedral coordination of cobalt is completed by two axial water molecules.

Synthesis and Crystal Structure of the Lead(II) Complex with 5-Hydroxyisophthalic Acid

2013 ◽  
Vol 634-638 ◽  
pp. 451-455
Author(s):  
Yan Yang ◽  
Liu Ting Yan ◽  
Rong Huan Qin ◽  
Wen Gui Duan
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Elemental Analysis ◽  
Three Dimensional ◽  
Single Crystal Diffraction ◽  
Intermolecular Hydrogen Bonds ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
3D Network ◽  
Hydrothermal Methods

The lead(II) Complex constructed with 5-hydroxyisophthalic acid, [Pb3(5-hipa)2]n•4H2O(1), (5-hipa = 5-hydro- xyisophthalic acid) has been synthesized by hydrothermal methods and structurally characterized by elemental analysis, IR and X-ray single crystal diffraction. In trinuclear symmetrical complex 1, Pb1 is four-coordinated, Pb2 and Pb3 are three-coordinated by 5-nitroisophthalic acid groups, respectively, which is further connected through intermolecular hydrogen bonds resulting in a three-dimensional (3D) network.

A Pyrazine-Bridged Ni(II) Coordination Polymer

2002 ◽  
Vol 57 (11) ◽  
pp. 1191-1194 ◽  
Author(s):  
Chirantan Roy Choudhury ◽  
Subrata Kumar Dey ◽  
Sutapa Sen ◽  
Bappaditya Bag ◽  
Samiran Mitra ◽  
...  
Keyword(s):  
Coordination Polymer ◽  
Chain Structure ◽  
Water Molecules ◽  
Polymeric Complex ◽  
X Ray Diffraction ◽  
Intermolecular Hydrogen Bonds ◽  
X Ray ◽  
Elemental Analyses ◽  
Coordinated Water ◽  
Nitrate Anions

The single pyrazine-bridged polymeric complex {[Ni(pyz)(H2O)4](NO3)2.2H2O}n has been synthesised and characterised by elemental analyses, IR and UV-vis spectra, and a single-crystal X-ray diffraction study. The coordination around the Ni centre is perfectly octahedral. The Ni(H2O)4 coordination planes are bridged by pyrazine ligands forming an infinite chain structure. Two nitrate anions and two water molecules exist in the lattice and are linked by intermolecular hydrogen bonds to the coordinated water molecules.

Synthesis, Structure and Characterization of a Novel Two-Dimensional Supramolecular Mn(II) Coordination Polymer Constructed from a 1,10-Phenanthroline Derivative and a Flexible Dicarboxylate

2010 ◽  
Vol 65 (9) ◽  
pp. 1173-1176 ◽  
Author(s):  
Zhi-Guo Kong ◽  
Xiao-Yuan Ma ◽  
Zhan-Lin Xu
Keyword(s):  
Ir Spectroscopy ◽  
Glutaric Acid ◽  
Title Complex ◽  
Two Dimensional ◽  
Crystal Data ◽  
X Ray Diffraction ◽  
Triclinic Space Group ◽  
X Ray ◽  
1D Chains

The title complex, [Mn2(glu)(L)2(HL)2]・0.5H2O (H2glu = glutaric acid, HL = 2-(2-chloro-6-fluorophenyl)-1Himidazo[ 4,5-f][1,10]phenanthroline) has been synthesized using a hydrothermal method and characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction. Crystal data: C162H88Cl8F8Mn4N32O9, triclinic, space group P1¯, a = 14.932(5), b = 16.414(5), c = 17.891(5) Å , α = 115.851(5), β = 91.288(5), γ = 112.894(5)◦, V = 3536.4(19) Å3, Z = 1. Compound 1 exhibits 1D chains which are further stacked by C-H...π interactions to give two-dimensional supramolecular layers.

Pentafluoro[(4-methyl-1,4-bisazoniacy clohex-1 -yl)methy 1] germanate Hydrate: Synthesis and Crystal Structure of a Zwitterionic λ6Ge-Germanate with a GeF5C Framework

1998 ◽  
Vol 53 (5-6) ◽  
pp. 535-539 ◽  
Author(s):  
Reinhold Tacke ◽  
Joachim Heermann ◽  
Melanie Pülm
Keyword(s):  
Molar Ratio ◽  
Water Molecules ◽  
Crystal Data ◽  
X Ray Diffraction ◽  
Coordination Polyhedra ◽  
Triclinic Space Group ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
Distorted Octahedra ◽  
Positively Charged

Abstract The zwitterionic (molecular) λ6Ge-germanate pentafluoro[(4-methyl-1,4-bisazoniacyclohexl-yl)methyl]germanate (5) was synthesized by reaction of 1-methyl-4-[(trimethoxygermyl) methyl]piperazine (8) with HF (molar ratio 1:5) in a mixture of water and ethanol at 0 °C and isolated as the hydrate 5 · H2O. The zwitterion 5 is characterized by the presence of a hexacoordinate (formally twofold negatively charged) germanium atom and two tetracoordinate (formally positively charged) nitrogen atoms. Compound 5 · H2O was structurally characterized by single-crystal X-ray diffraction. Crystal data are as follows: C6H17F5GeN2O , triclinic space group P1̄ (no. 2), a = 7.5228(11) Å, b = 12.174(2) Å, c = 12.3041(14) Å, α = 73.74(2)°, β = 82.44(2)°, γ = 74.762(10)°, V = 1041.7(2) Å3, T = 173(2) K, Z = 4, R1 = 0.0227. There are one pair each of crystallographically independent zwitterions 5 and water molecules in the asymmetric unit, the structures of the zwitterions being very similar. Their coordination polyhedra around the germanium atoms are slightly distorted octahedra.

scholarly journals Crystal structure of cis-(1,4,8,11-tetraazacyclotetradecane-κ4 N)bis(thiocyanato-κN)chromium(III) bromide from synchrotron X-ray diffraction data

2021 ◽  
Vol 77 (3) ◽  
pp. 222-225
Author(s):  
Dohyun Moon ◽  
Jong-Ha Choi
Keyword(s):  
Crystal Structure ◽  
Complex Cation ◽  
Title Complex ◽  
Asymmetric Unit ◽  
X Ray Diffraction ◽  
Intermolecular Hydrogen Bonds ◽  
X Ray ◽  
Bromide Anion ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral

The crystal structure of the title complex, cis-[Cr(NCS)2(cyclam)]Br (cyclam = 1,4,8,11-tetraazacyclotetradecane, C10H24N4), has been determined from synchrotron X-ray data. The asymmetric unit contains one [Cr(NCS)2(cyclam)]+ cation and one bromide anion. The CrIII ion of the complex cation is coordinated by the four N atoms of the cyclam ligand and by two N-coordinating NCS groups in a cis arrangement, displaying a distorted octahedral coordination sphere. The Cr—N(cyclam) bond lengths are in the range 2.075 (3) to 2.081 (3) Å while the average Cr—N(NCS) bond length is 1.996 (16) Å. The macrocyclic cyclam moiety adopts the most stable cis-V conformation. The crystal structure is stabilized by intermolecular hydrogen bonds involving the cyclam N—H groups as donor groups, and the bromide anion and the S atom of one of the NCS ligands as acceptor groups.

scholarly journals Structure of triaquatris(1,1,1-trifluoro-4-oxopentan-2-olato)cerium(III) as a possible fluorescent compound

2018 ◽  
Vol 74 (2) ◽  
pp. 229-232
Author(s):  
Atsuya Koizumi ◽  
Takuya Hasegawa ◽  
Atsushi Itadani ◽  
Kenji Toda ◽  
Taoyun Zhu ◽  
...  
Keyword(s):  
Title Complex ◽  
Water Molecules ◽  
Two Dimensional ◽  
Bidentate Ligands ◽  
Intermolecular Hydrogen Bonds ◽  
Fluorescent Compound ◽  
Organic Complexes ◽  
Metal Metal ◽  
Metal Organic ◽  
Monodentate Ligands

Luminescence due to the d–f transition of Ce3+ is quite rare in metal–organic complexes where concentrate quenching frequently occurs. One of the possible ways to avoid this is to design an architecture with elongated metal–metal distances. In the structure of the title complex, triaquatris(1,1,1-trifluoro-4-oxopentan-2-olato-κ2 O,O′)cerium(III), [Ce(C5H4F3O2)3(H2O)3], the CeIII complex is linked to neighbouring ones by hydrogen bonding. Within the complex, the CeIII atom is coordinated by nine O atoms from three 1,1,1-trifluoro-4-oxopentan-2-olate (tfa) anions as bidentate ligands and three water molecules as monodentate ligands. Thus, the coordination number of CeIII atom is nine in a monocapped square–antiprismatic polyhedron. The F atoms of all three independent CF3 groups in tfa are disordered over two positions with occupancy ratios of about 0.8:0.2. The intermolecular hydrogen bonds between the ligands involve tfa–water interactions along the [110] and [1-10] directions, generating an overall two-dimensional layered network structure. The presence of the F atoms in the tfa anion is responsible for an increased intermolecular metal–metal distance compared to that in the analogous acetylacetonate (acac) derivatives. Fluorescence from Ce3+ is, however, not observed.

scholarly journals An infinite two-dimensional hybrid water–chloride network in a 4′-(furan-2-yl)-2,2′:6′,2′′-terpyridine nickel(II) matrix

2017 ◽  
Vol 73 (6) ◽  
pp. 871-875 ◽  
Author(s):  
Wei-Wei Fu ◽  
Ya-Qian Li ◽  
Yang Liu ◽  
Man-Sheng Chen ◽  
Wei Li ◽  
...  
Keyword(s):  
Hydrogen Bonds ◽  
Chloride Ions ◽  
Water Molecules ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Coordination Environment ◽  
X Ray ◽  
Solvent Water ◽  
Distorted Octahedral ◽  
Shaped Pattern

A new complex, namely bis[4′-(furan-2-yl)-2,2′:6′,2′′-terpyridine]nickel(II) dichloride decahydrate, [Ni(C19H13N3O)2]Cl2·10H2O, has been crystallized by solvent evaporation and characterized by single-crystal X-ray diffraction. The coordination environment of the NiIIcation is distorted octahedral with slight deviations from an idealized geometry. The most intriguing structural feature is an infinite two-dimensional hybrid water–chloride network parallel to (011) constructed by O—H...O and O—H...Cl hydrogen bonds involving two independent chloride ions and ten independent solvent water molecules with an L-shaped pattern. One of the furyl rings is disordered with a refined occupancy ratio of 0.786 (13):0.214 (13)

Synthesis and Crystal Structure of the Cobalt (II) Complex with Mixed-Ligand

2011 ◽  
Vol 418-420 ◽  
pp. 59-62
Author(s):  
Yan Yang ◽  
Liu Ting Yan ◽  
Xiao Li ◽  
Rong Huan Qin ◽  
Wen Gui Duan
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Mixed Ligand ◽  
Single Crystal Diffraction ◽  
Intermolecular Hydrogen Bonds ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
3D Network ◽  
Hydrothermal Methods

The Cobalt (Ⅱ) Complex constructed with 5-nitroisophthalic acid and 2,2’-bibenzimidazole, [Co(H2bibim)2( 5-nipa)] (1), (H2bibim =2,2’-bibenzimidazole, 5-nipa=5-nitroisophthalic acid) have been synthesized by hydrothermal methods and structurally characterized by elemental analysis, IR and X-ray single crystal diffraction. Complex 1 has six coordinated by two H2bibim ligands and one 5-nitroisophthalic acid groups that is further connected though intermolecular hydrogen bonds and resulting in a three-dimensional (3D) network.

scholarly journals Unusual potassium-oxalate coordination in the two-dimensional trimetallic [CoCl(NH3)5][KCr(C2O4)3]·0.5H2O complex

2014 ◽  
Vol 12 (6) ◽  
pp. 652-658 ◽  
Author(s):  
Grzegorz Wrzeszcz ◽  
Andrzej Wojtczak ◽  
Magdalena Zawadzka
Keyword(s):  
Variable Temperature ◽  
Water Molecules ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Potassium Oxalate ◽  
Hydrogen Atoms ◽  
X Ray ◽  
Variable Temperature Magnetic Susceptibility ◽  
Different Types ◽  
Heterometallic Compound

AbstractA new heterometallic compound, [CoCl(NH3)5][KCr(C2O4)3]·0.5H2O (1), has been synthesized and characterized by elemental analysis, IR and electronic spectra, thermal analysis, variable temperature magnetic susceptibility measurements, and single crystal X-ray diffraction. Compound 1 consists of two-dimensional [{KCr(C2O4)3}n]2n− layers, [CoCl(NH3)5]2+ ions and water molecules. Within the 2-D layer, three different types of oxalate coordination modes are present. Each K cation is coordinated by eight oxygen atoms from oxalate groups and also weakly interacts with the ninth oxygen atom. The extensive network of hydrogen bond is formed between the [KCr(C2O4)3]2− layer and the [CoCl(NH3)5]2+ ions. These interactions involve all hydrogen atoms of ammonia ligads and water molecule.

Cyclophan-Metall-Komplexe: Synthese und Kristallstruktur von ([2](l,4)Naphthalino[2]paracyclophan)gallium(I)-tetrabromogallat(III)/Cyclophane Metal Complexes: Synthesis and Crystal Structure of ([2]( 1,4)Naphthalino[2]paracyclophane)gallium(I) Tetrabromogallate(III)

1987 ◽  
Vol 42 (2) ◽  
pp. 147-150 ◽  
Author(s):  
H. Schmidbaur ◽  
W. Bublak ◽  
G. Müller
Keyword(s):  
Crystal Structure ◽  
Metal Complexes ◽  
Single Crystal ◽  
Benzene Ring ◽  
Title Complex ◽  
Outer Side ◽  
X Ray Diffraction ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
Secondary Reactions

AbstractThe title complex has been prepared from Ga[GaBr4] and [2](1,4)naphthalino[2]paracyclophane in toluene as a solvent, and the crystal structure of this adduct determined by single crystal X-ray diffraction. The structure is composed of dimeric units Ga2[GaBr4]2 , which are crosslinked into sheets through Ga(I)-arene coordination. Both the benzene ring and the substituted ring of the naphthalene system are η6-bonded from the outer side of the cyclophane cage, each to an univalent metal. The benzene and the naphthalene form an interplane angle of 49.3°. The distance to the benzene ring (2.67 Å) is much shorter than the distance to the naphthalene (2.85 Å), suggesting a stronger complexation with the unperturbed π-system of the former. [2.2](l,4)Naphthalinophane forms no adduct with Ga[GaBr4], and with [2](l,5)naphthalino[2]paracyclophane secondary reactions are observed.

Sign in / Sign up

Export Citation Format

Share Document