Luminescent and magnetic bifunctional coordination complex based on a chiral tartaric acid derivative and europium

2019 ◽  
Vol 75 (9) ◽  
pp. 1220-1227 ◽  
Author(s):  
Mei-rong Han ◽  
Shao-dong Li ◽  
Ling Ma ◽  
Bang Yao ◽  
Si-Si Feng ◽  
...  
Keyword(s):  
Tartaric Acid ◽  
Complex I ◽  
Coupling Parameter ◽  
Chain Structure ◽  
Magnetic Behaviour ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Carboxylate Groups ◽  
The Eu

A new mononuclear europium complex incorporating the (+)-di-p-toluoyl-D-tartaric acid (D-H2DTTA) ligand, namely, catena-poly[tris{μ2-3-carboxy-2,3-bis[(4-methylphenyl)carbonyloxy]propanoato}tris(methanol)europium(III)], [Eu(C20H17O8)3(CH3OH)3] n , (I), has been synthesized and characterized by IR spectroscopy, elemental analysis, powder X-ray diffraction and single-crystal X-ray diffraction analysis. The structure analysis indicates that complex (I) crystallizes in the trigonal space group R3 and exhibits an infinite one-dimensional chain structure, in which the Eu3+ ion is surrounded by six O atoms from six D-HDTTA− ligands and three O atoms from three coordinated methanol molecules, thus forming a tricapped trigonal prism geometry. The D-H2DTTA ligand is partially deprotonated and adopts a μ1,6-coordination mode via two carboxylate groups to link adjacent Eu3+ ions, affording an infinite one-dimensional propeller-shaped coordination polymer chain along the c axis, with an Eu...Eu distance of 7.622 (1) Å. Moreover, C—H...π interactions lead to the formation of helical chains running along the c axis and the whole structure displays a snowflake pattern in the ab plane. The circular dichroism spectrum confirms the chirality of complex (I). The solid-state photoluminescence properties were also investigated at room temperature and (I) exhibits characteristic red emission bands derived from the Eu3+ ion (CIE 0.63, 0.32), with a reasonably long lifetime of 0.394 ms, indicating effective energy transfer from the ligand to the metal centre. In addition, a magnetic investigation reveals single-ion magnetic behaviour. The spin-orbit coupling parameter (λ) between the ground and excited states is fitted to be 360 (2) cm−1 through Zeeman perturbation. Therefore, complex (I) may be regarded as a chiral optical-magneto bifunctional material.

Preparation and Structural Characterization of Chain Ni (II) Coordination Polymer Material

2011 ◽  
Vol 322 ◽  
pp. 369-372
Author(s):  
Zhi Xiang Ji
Keyword(s):  
Coordination Polymer ◽  
Polymer Material ◽  
Chain Structure ◽  
Monoclinic Space Group ◽  
Dimensional Chain ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
A Chain

A chain Ni (II) coordination polymer material was prepared and characterized by elemental analysis and single-crystal X-ray diffraction. It crystallizes in monoclinic, space group C2/c with a = 1.24348(13) nm, b = 1.29477(12) nm, c = 1.51480(17) nm and Dc = 1.401 g•cm-3. The results of structural analysis indicated that each Ni (II) ion forms six-coordinated with nitrogen atoms of pyridine and thiocyanate, and the Ni (II) coordination polymer material formed one dimensional chain structure by the interaction of pyridine rings.

A one-dimensional coordination polymer with a three-dimensional supramolecular framework:catena-poly[[[(3,4,7,8-tetramethyl-1,10-phenanthroline)cadmium(II)]-μ3-4,4′-sulfonyldibenzoato] trihydrate]

2013 ◽  
Vol 69 (3) ◽  
pp. 241-243 ◽  
Author(s):  
Jun Wang ◽  
Jian-Qing Tao ◽  
Xiao-Juan Xu ◽  
Chun-Yun Tan
Keyword(s):  
Three Dimensional ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Polymeric Compound ◽  
Chain Polymer ◽  
One Dimensional ◽  
X Ray ◽  
Carboxylate Groups ◽  
Metal Organic ◽  
Coordination Patterns

In the title mixed-ligand metal–organic polymeric compound, {[Cd(C14H8O6S)(C16H16N2)]·3H2O}n, the asymmetric unit contains a crystallographically unique CdIIatom, one doubly deprotonated 4,4′-sulfonyldibenzoic acid (H2SDBA) ligand, one 3,4,7,8-tetramethyl-1,10-phenanthroline (TMPHEN) molecule and three solvent water molecules. Each CdIIcentre is six-coordinated by two O atoms from a chelating carboxylate group of a SDBA2−ligand, two O atoms from monodentate carboxylate groups of two different SDBA2−ligands and two N atoms from a chelating TMPHEN ligand. There are two coordination patterns for the carboxylate groups of the SDBA2−ligand, with one in a μ1-η1:η1chelating mode and the other in a μ2-η1:η1bis-monodentate mode. Single-crystal X-ray diffraction analysis revealed that the title compound is a one-dimensional double-chain polymer containing 28-membered rings based on the [Cd2(CO2)2] rhomboid subunit. More interestingly, a chair-shaped water hexamer cluster is observed in the compound.

Synthesis, Crystal Structure and Antibacterial Activity of 1D Chain Ca(II) Coordination Polymer

2011 ◽  
Vol 282-283 ◽  
pp. 96-99
Author(s):  
Xi Shi Tai
Keyword(s):  
Crystal Structure ◽  
Antibacterial Activity ◽  
Coordination Polymer ◽  
Chain Structure ◽  
Molar Conductance ◽  
Dimensional Chain ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
1D Chain

1D chain Ca(II) coordination polymer was synthesized and characterized by elemental analysis, molar conductance, IR and single-crystal X-ray diffraction, The results of crystal structure show that each Ca(II) ion forms eight-coordinated and the complex formed one dimensional chain structure by the oxygen atoms of carboxylate and water bridged. The antibacterial activity of the Ca(II) coordination polymer and the ligand were tested, the results show that the complex show considerable antibacterial activity against escherichia coli, bacillus subtilis and staphylococcus white.

A one-dimensional coordination polymer based on Cd2O2clusters: poly[aqua(μ3-4,4′-sulfonyldibenzoato)(3,4,7,8-tetramethyl-1,10-phenanthroline-κ2N,N′)cadmium(II)]

2013 ◽  
Vol 69 (3) ◽  
pp. 244-246 ◽  
Author(s):  
Jian-Qing Tao
Keyword(s):  
Water Molecule ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Chain Polymer ◽  
One Dimensional ◽  
X Ray ◽  
Acid Ligand ◽  
Carboxylate Groups ◽  
Metal Organic ◽  
Coordinated Water

In the title mixed-ligand metal–organic polymeric complex [Cd(C14H8O6S)(C16H16N2)(H2O)]n, the asymmetric unit contains a crystallographically unique CdIIatom, one doubly deprotonated 4,4′-sulfonyldibenzoic acid ligand (H2SDBA), one 3,4,7,8-tetramethyl-1,10-phenanthroline (TMPHEN) molecule and one water molecule. Each CdIIcentre is coordinated by two N atoms from the chelating TMPHEN ligand, three O atoms from monodentate carboxylate groups of three different SDBA2−ligands and one O atom from a coordinated water molecule, giving a distorted CdN2O4octahedral geometry. Single-crystal X-ray diffraction analysis reveals that the compound is a one-dimensional double-chain polymer containing 28-membered rings based on Cd2O2clusters, with a Cd...Cd separation of 3.6889 (4) Å. These chains are linked by O—H...O and C—H...O hydrogen bonds to form a three-dimensional supramolecular framework. The framework is reinforced by π–π and C—O...π interactions.

Synthesis, crystal structure and fluorescence spectrum of a cadmium(II) sulfaquinoxaline complex

2013 ◽  
Vol 69 (11) ◽  
pp. 1332-1335 ◽  
Author(s):  
Xiu-Hua Zhao ◽  
Ya-Yun Zhao ◽  
Jie Zhang ◽  
Jian-Guo Pan ◽  
Xing Li
Keyword(s):  
Thermal Analysis ◽  
Single Crystal ◽  
Fluorescence Spectrum ◽  
Chain Structure ◽  
Zigzag Chain ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Distorted Octahedral Coordination Geometry ◽  
Distorted Octahedral

catena-Poly[[[4-amino-N-(quinoxalin-2-yl)benzenesulfonamidato]aquacadmium(II)]-μ-4-amino-N-(quinoxalin-2-yl)benzenesulfonamidato], [Cd(C14H11N4O2S)2(H2O)], has been synthesized hydrothermally and characterized by single-crystal X-ray diffraction, elemental analysis, fluorescence, IR and thermal analysis. Single-crystal X-ray analysis reveals that the complex is a one-dimensional zigzag chain structure, and the CdIIcation has a distorted octahedral coordination geometry formed by five N atoms from three different sulfaquinoxaline ligands and one O atom from a water molecule. The fluorescence spectrum reveals that the complex emits strong blue fluorescence and thermal analysis shows that the complex has high thermal stability.

Research on the Structure of One-Dimensional Chain Calcium (ΙΙ) Complex Material

2011 ◽  
Vol 366 ◽  
pp. 400-403
Author(s):  
Li Hua Wang
Keyword(s):  
Single Crystal ◽  
Calcium Ion ◽  
Chain Structure ◽  
Monoclinic Space Group ◽  
Dimensional Chain ◽  
X Ray Diffraction ◽  
Complex Material ◽  
One Dimensional ◽  
X Ray ◽  
Π Stacking Interaction

A new Ca(II) complex material has been prepared by the reaction of calcium perchlorate with 4-amino-3-methyl-benzenesulfonic acid and sodium hydroxide, and was characterized by single-crystal X-ray diffraction. The results showed that the complex crystallizes in monoclinic, space group P2(1)/n with a = 0.63090(10) nm, b = 0. 70513(11) nm, c = 2.4262(4) nm, V = 1.0766(3) nm3, Z = 2, F (000) = 562, Rint = 0.0252. Single-crystal X-ray diffraction analysis revealed that each calcium ion lies in six-coordinated environments, and the complex formed one dimensional chain structure through intramolecule and intermolecule hydrogen bonds and π-π stacking interaction.

Synthesis, crystal structures and magnetic characterisation of two 2p–3d metallic coordination polymers

2017 ◽  
Vol 41 (6) ◽  
pp. 365-369 ◽  
Author(s):  
Chongchong Xue ◽  
Jingwen Shi ◽  
Daopeng Zhang
Keyword(s):  
Magnetic Susceptibility ◽  
Coordination Polymers ◽  
Supramolecular Structure ◽  
Three Dimensional ◽  
Building Blocks ◽  
Chain Structure ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Dimensional Network

The coordination polymers {Mg[Fe(L)(CN)5]}n·0.5nH2O and {MgCu2(CH3COO)6}n [L = bis( N-imidazolyl)methane] have been synthesised. X-ray diffraction revealed that {Mg[Fe(L)(CN)5]}n·0.5nH2O has a one-dimensional neutral chain structure consisting of alternating [Mg(L)2(H2O)2)]2+ species and [Fe(L)(CN)5]2– building blocks, which can be further linked into a three-dimensional supramolecular structure by inter-chain p–p interactions. {MgCu2(CH3COO)6}n has a three-dimensional network with the [MgCu2(CH3COO)6] unit as neutral core extended by Mg–O bonds. Magnetic susceptibility studies on {MgCu2(CH3COO)6}n revealed antiferromagnetic interactions between adjacent Cu(II) ions.

Syntheses, Structures and Properties of a Cobalt(II) and a Cadmium(II) Complex Based on 1-((Benzotriazol-1-yl)methyl)-1H-1,3-imidazole and 1,3-Benzenedicarboxylate Ligands

2014 ◽  
Vol 69 (4) ◽  
pp. 423-431 ◽  
Author(s):  
Qiuying Huang ◽  
Weiping Tang ◽  
Yi Yang ◽  
Wei Liu
Keyword(s):  
Ir Spectra ◽  
Single Crystal ◽  
Layered Structure ◽  
Chain Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carboxylate Groups ◽  
Benzenedicarboxylic Acid ◽  
Structures And Properties ◽  
A Chain

Two new complexes with the formulae {[Co(bmi)2(bdc)(H2O)]·2H2O}n (1) and {[Cd(bmi)(bdc) (H2O)]·DMF}n (2) (bmi = 1-((benzotriazol-1-yl)methyl)-1H-1,3-imidazole, H2bdc = 1,3-benzenedicarboxylic acid) have been synthesized and characterized by single-crystal X-ray diffraction. Complex 1 exhibits a chain structure in which both carboxylate groups of each 1,3-benzenedicarboxylate coordinate to the Co(II) ions in monodentate and chelating modes, and the bmi ligands with a monodentate mode. Complex 2 features a layered structure where both carboxylate groups of each 1,3- benzenedicarboxylate coordinate to the Cd(II) ions in monodentate and chelating modes, but the bmi ligands with a bridging mode. The IR spectra, PXRD patterns, thermogravimetric analyses, and fluorescence properties are also presented.

Cd and Hg coordination complexes based on a heterocyclic multidentate ligand: Synthesis, structures and photoluminescence properties

2017 ◽  
Vol 41 (5) ◽  
pp. 275-279
Author(s):  
Jiyong Hu ◽  
Fan Yang ◽  
Jin'an Zhao
Keyword(s):  
Single Crystal ◽  
Coordination Complexes ◽  
Chain Structure ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Multidentate Ligand ◽  
The Third ◽  
Binuclear Structure

The complexes [Cd(cpbi)Cl2]·(H2O), [Hg2(cpbi)2Cl4] and [Hg(cpbi)Br2] (cpbi = [5-chloro-2-(pyrazin-2-yl)-1H-benzoimidazole]) have been synthesised using solvent evaporation reactions and structurally characterised by single-crystal X-ray diffraction. The first complex displays a one-dimensional (1-D) chain structure, the second has a binuclear structure, while the third is mononuclear. The complexes show different luminescence properties.

Synthesis and Structural Characterization of Zn(II) Coordination Polymer Material

2011 ◽  
Vol 282-283 ◽  
pp. 100-103 ◽  
Author(s):  
Li Hua Wang
Keyword(s):  
Hydrogen Bond ◽  
Coordination Polymer ◽  
Chain Structure ◽  
Title Complex ◽  
Dimensional Chain ◽  
X Ray Diffraction ◽  
Monoclinic System ◽  
One Dimensional ◽  
X Ray

In order to synthesize a new catalysis material, the title complex, [Zn(2,2’-bipyridine)(H2O)2(SO4)]n, was prepared and determined by X-ray diffraction. The results shows that the compound was crystallized in the monoclinic system, space groupC2/c, witha= 15.4304(14) Å,b= 12.7150(11) Å,c= 6.7068(5) Å,β= 102.103(10)º,V= 1286.61(19) Å3,Z= 4. The geometry of Zn(II) is a distortedcis-ZnN2O4octahedron. In the structure of the title complex, a one-dimensional chain structure is formed by hydrogen-bond.

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