Syntheses, Structures, Thermal and Photoluminescence Properties of Two Zn(II) and Cd(II) Coordination Polymers Constructed from Taurine-derived Schiff Base and 4,4’-Bipyridine Ligands

2012 ◽  
Vol 67 (8) ◽  
pp. 774-782 ◽  
Author(s):  
Wei-Ting Guo ◽  
Zhi-Min Miao ◽  
Yun-Long Wang
Keyword(s):  
Schiff Base ◽  
Coordination Polymers ◽  
Tridentate Ligand ◽  
Supramolecular Architecture ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
Monodentate Ligand ◽  
Metal Centers ◽  
X Ray ◽  
Ethanesulfonic Acid

Two chain-like coordination polymers, namely, {[Zn(saes)(4,4'-bipy)(H2O)]·H2O}n (1) and {[Cd (Hsaes)2(4,4'-bipy)(H2O)2]·2H2O}n (2), where H2saes=2-(2-hydroxybenzylideneamino)ethanesulfonic acid and 4,4'-bipy=4,4'-bipyridine, have been synthesized and characterized by singlecrystal X-ray diffraction, IR spectroscopy, elemental, thermogravimetric and photoluminescence analysis. X-Ray diffraction analyses indicate that 1and 2display octahedral metal centers with N3O3 and N2O4 donor sets, respectively. The Schiff base serves as a common N,O'-tridentate ligand in 1, and as a unique O-monodentate ligand in 2. In the crystal, both 1and 2form a 3D supramolecular architecture by O-H···O, C-H···O interactions or π···π stacking. The thermal and solid-state photoluminescence properties of both complexes have been investigated

A New 2D Copper(II) Coordination Polymer with a Schiff Base Ligand with Weakly Coordinating Sulfonate Groups Affecting the Structure

2012 ◽  
Vol 67 (1) ◽  
pp. 11-16
Author(s):  
Jia-Ming Li ◽  
Kun-Huan He ◽  
Yi-Min Jiang
Keyword(s):  
Schiff Base ◽  
Thermogravimetric Analysis ◽  
Coordination Polymer ◽  
Schiff Base Ligand ◽  
Copper Complexes ◽  
Building Blocks ◽  
Supramolecular Architecture ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ethanesulfonic Acid

A new 2D copper(II) coordination polymer with the doubly deprotonated Schiff base ligand 2- (2-hydroxybenzylideneamino)ethanesulfonic acid (H2Saes) has been synthesized, {[Cu(Saes)(4,4´- bpy)]2·H2O}n (1), and characterized by single-crystal X-ray diffraction, IR spectroscopy, elemental and thermogravimetric analysis. Dinuclear copper complexes serve as secondary building blocks (SBUs) to construct an unusual coordination network with an interpenetrating CdSO4 topology. In the crystal, the components form a stable 3D supramolecular architecture by O-H· · ·O, C-H· · ·O interactions and π stacking.

scholarly journals Synthesis and structural peculiarities of gallium Complexes with novel paullone derivatives

2008 ◽  
Vol 6 (3) ◽  
pp. 340-346 ◽  
Author(s):  
Werner Ginzinger ◽  
Vladimir Arion ◽  
Gerald Giester ◽  
Markus Galanski ◽  
Bernhard Keppler
Keyword(s):  
Schiff Base ◽  
Tridentate Ligand ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gallium Chloride ◽  
Structural Peculiarities ◽  
Gallium Complex ◽  
Gallium Complexes

Abstract9-Bromo-7,12-dihydroindolo[3,2-d][1]benzazepin-6-ylhydrazine was reacted with 2-acetylpyridine to give a Schiff base as a potential tridentate ligand. The reaction of this ligand with gallium chloride afforded complexes of 1:1 and 2:1 stoichiometry. The results of X-ray diffraction studies of the ligand and both gallium complexes are reported and compared with the data for a related gallium complex with a Schiff base obtained from 9-bromo-7,12-dihydroindolo[3,2-d][1]benzazepin-6-ylhydrazine and 2-hydroxybenzaldehyde.

Three Coordination Polymers Built by Methoxyphenyl Imidazole Dicarboxylate: Solvothermal Syntheses, Crystal Structures, and Properties

2015 ◽  
Vol 68 (6) ◽  
pp. 956 ◽  
Author(s):  
Ming-An Dang ◽  
Zi-Feng Li ◽  
Ying Liu ◽  
Gang Li
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
Bridging Ligands ◽  
X Ray ◽  
Structures And Properties ◽  
Solvothermal Syntheses ◽  
Lattice Polymer ◽  
Imidazole Dicarboxylate

Three coordination polymers [Sr(p-H2MOPhIDC)2]n (1) (p-H3MOPhIDC = 2-p-methoxyphenyl-1H-imidazole-4,5-dicarboxylic acid), {[Cd2(p-HMOPhIDC)2(4,4′-bipy)]⋅H2O}n (4,4′-bipy = 4,4′-bipyridine) (2), and [Zn(p-HMOPhIDC)(4,4′-bipy)]n (3) have been solvothermally synthesized, and structurally characterized by single-crystal X-ray diffraction. Polymer 1 indicates a three-dimensional framework, which can be simplified as a 6-connected lattice. Polymer 2 is also a three-dimensional framework, and contains mixed bridging ligands HMOPhIDC2– and 4,4′-bipy. Polymer 3 exhibits a sheet structure bearing infinite rectangles. The coordination modes of the p-H3MOPhIDC ligand, and the thermal and solid-state photoluminescence properties of the polymers have been investigated as well.

scholarly journals Three New Supramolecular Coordination Polymers Based on 1H-pyrazolo[3,4-b]pyridin-3-amine and 1,3-benzenedicarboxylate Derivatives

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 819 ◽  
Author(s):  
Yun Xu ◽  
Qing-Hua Deng ◽  
Fang Ding ◽  
Ran An ◽  
Dong Liu ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Coordination Polymers ◽  
Supramolecular Network ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrogen Bonding Interactions ◽  
Sheet Structure ◽  
Supramolecular Coordination ◽  
Solvothermal Conditions

Three new supramolecular coordination polymers, namely [Zn(1,3-BDC)(HL)]n (Polymer 1), [Zn3(1,3,5-BTC)2(HL)2(H2O)2]n (Polymer 2), and [Zn9(5-SO3-1,3-BDC)2(L)8(OH)4]n (Polymer 3), were synthesized under solvothermal conditions, based on 1H-pyrazolo[3,4-b]pyridin-3-amine (HL) along with 1,3-benzenedicarboxylate (1,3-BDC) and its derivatives, such as 1,3,5-benzenetricarboxylate (1,3,5-BTC) and 5-sulfo-1,3-benzenedicarboxylate (5-SO3-1,3-BDC). Polymers 1–3 were characterized by elemental analysis, IR spectroscopy, powder X-ray diffraction (PXRD), and single crystal X-ray diffraction analysis. Polymer 1 exhibited a two-dimensional (2D) 4-connected sql net. The neighboring 2D nets were further linked into a 3D supramolecular network by hydrogen-bonding interactions. Polymer 2 displayed a 3D (4, 4, 4)-connected network, which was further stabilized by R 2 2 (14) and S(9) hydrogen-bonding rings along with π–π interactions. The 2D sheet structure of Polymer 3 was constructed by novel quasi-linear nonanuclear Zn(II) units, which further extended into a 3D supramolecular structure by hydrogen-bonding interactions. The solid-state photoluminescence properties of Polymers 1–3 were also investigated.

scholarly journals Heterometallic CoIIIZnII Schiff Base Catalyst for Mild Hydroxylation of C(sp3)–H Bonds of Unactivated Alkanes: Evidence for Dual Mechanism Controlled by the Promoter

Catalysts ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 209 ◽  
Author(s):  
Oksana Nesterova ◽  
Katerina Kasyanova ◽  
Elena Buvaylo ◽  
Olga Vassilyeva ◽  
Brian Skelton ◽  
...  
Keyword(s):  
Schiff Base ◽  
Nitric Acid ◽  
Schiff Base Complex ◽  
Zinc Powder ◽  
The Novel ◽  
X Ray Diffraction ◽  
Turnover Number ◽  
Metal Centers ◽  
X Ray ◽  
Dual Mechanism

The novel Schiff base complex [CoIIIZnIIL3Cl2]·CH3OH (1) was synthesized by interaction of zinc powder, cobalt(II) chloride and methanol solution of the pre-formed HL in air (HL is the product of condensation of o-vanillin and methylamine) and characterized by IR, UV-Vis and NMR spectroscopy, ESI-MS and single crystal X-ray diffraction analysis. In the heterometallic core of 1 the two metal centers are bridged by deprotonated phenoxy groups of the L− ligands with the cobalt-zinc separation of 3.123 Å. Catalytic investigations demonstrated a pronounced activity of 1 towards mild alkane oxidation with m-chloroperbenzoic acid (m-CPBA) as an oxidant and cis-1,2-dimethylcyclohexane (cis-1,2-DMCH) as the model substrate. The influence of the nature of different promoting agents of various acidities (from HOTf to pyridine) on the catalytic process was studied in detail and a pronounced activity of 1 in the presence of nitric acid promoter was found, also showing a high retention of stereoconfiguration of the substrate (>99% for cis-1,2-DMCH). The best achieved yield of tertiary cis-alcohol based on the oxidant was 61%, with a turnover number (TON) of 198 for nitric acid as promoter. The 18O-incorporations into the alcohols when the reactions were performed under 18O2 atmosphere using acetic and nitric acid promoters, suggest that the cis-1,2-DMCH hydroxylation proceeds by two distinct pathways, a non-stereoselective and a stereoselective one (with and without involvement of a long-lived free carbon radical, respectively). The former dominates in the case of acetic acid promoter and the latter is realized in the case of HNO3 promoter.

Syntheses and structural studies of η5-pentamethylcyclopentadienyl rhodium(III) and iridium(III) complexes of a Schiff-base expanded porphyrin

2010 ◽  
Vol 14 (01) ◽  
pp. 41-46 ◽  
Author(s):  
Luciano Cuesta ◽  
Vincent M. Lynch ◽  
Jonathan L. Sessler
Keyword(s):  
Schiff Base ◽  
Intramolecular Hydrogen Bonding ◽  
X Ray Diffraction ◽  
Nmr Studies ◽  
Coordination Environment ◽  
Metal Centers ◽  
X Ray ◽  
Hydrogen Bonding Interactions ◽  
Intramolecular Hydrogen ◽  
Expanded Porphyrin

Reported here is the synthesis of new binuclear rhodium(III) and iridium(III) semi-sandwich complexes of a Schiff-base expanded porphyrin. Single crystals of these new complexes were subject to X-ray diffraction analysis. The resulting structures revealed that the Schiff-base macrocycle adopts a V-shape in which two {(η5- C 5 Me 5) MCl } ( M = Rh and Ir ) fragments are accommodated within the macrocyclic pocket. The coordination environment of the metal centers is typical to that of "piano stool"-type complexes. The X-ray analyses and complementary NMR studies (carried out in CD 2 Cl 2) provide evidence for the existence of strong intramolecular hydrogen-bonding interactions between the pyrrolic NH protons and the chloride counteranion both in solution and in the solid state.

Synthesis, crystal structures and characterizations of two homochiral coordination polymers based on a chiral reduced Schiff base ligand

2014 ◽  
Vol 70 (4) ◽  
pp. 375-378 ◽  
Author(s):  
Shao-Ming Ying ◽  
Xiao-Hui Huang ◽  
Wu-Kui Luo ◽  
Yan-Chun Xiao
Keyword(s):  
Schiff Base ◽  
Coordination Polymers ◽  
Schiff Base Ligand ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Strong Emission ◽  
X Ray ◽  
Dimensional Network ◽  
Elemental Analyses ◽  
Reduced Schiff Base

Two homochiral coordination polymers based on a chiral reduced Schiff base ligand, namely poly[(μ5-4-{[(NR,1S)-(1-carboxylato-2-phenylethyl)amino]methyl}benzoato)zinc(II)], [Zn(C17H15NO4)]n, (1), and poly[(μ5-4-{[(NR,1S)-(1-carboxylato-2-phenylethyl)amino]methyl}benzoato)cobalt(II)], [Co(C17H15NO4)]n, (2), have been obtained by hydrothermal methods and studied by single-crystal X-ray diffraction, elemental analyses, powder X-ray diffraction, thermogravimetric analysis, IR spectroscopy and fluorescence spectroscopy. Compounds (1) and (2) are isostructural and crystallize in theP212121space group. Both display a three-dimensional network structure with a one-dimensional channel, with the benzyl group of the ligand directed towards the channel. An investigation of photoluminescence properties shows that compound (1) displays a strong emission in the purple region.

Two 1D zinc coordination polymers based on tris(p-carboxylphenyl)phosphine oxide: syntheses, structures and photoluminescence properties

2017 ◽  
Vol 72 (8) ◽  
pp. 579-584 ◽  
Author(s):  
Feng Da Bao ◽  
Ya Jie Ruan ◽  
Ge Ge Du ◽  
Shu Kai Zou ◽  
Jie Zhang ◽  
...  
Keyword(s):  
Solid State ◽  
Coordination Polymers ◽  
Phosphine Oxide ◽  
Elemental Analysis ◽  
Structural Features ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metal Organic ◽  
Zinc Coordination

AbstractTwo metal-organic coordination polymers constructed from tris(p-carboxylphenyl)phosphine oxide (TPOH3), namely, [Zn(TPOH)(2,2′-bipy)(H2O)·H2O·DMF]n (1) and [Zn2(TPOH)2(1,4-bix)2·5H2O]n (2) (2,2′-bipy=2,2′-bipydine, 1,4-bix=1,4-bis(imidazol-1-ylmethyl)benzene), were synthesized and identified by IR, elemental analysis and single-crystal X-ray diffraction analysis. Both of the 2,2′-bipy and 1,4-bix ligands tailor the complexes 1 and 2 into chain structures. The thermal behavior and solid state photoluminescence properties correlated with the corresponding structural features were investigated.

Two luminescent d10 metal coordination polymers based on 3-nitro-5-(pyridin-3-yl)benzoic acid

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Long Tang ◽  
HuanHuan Wang ◽  
YuHao Fu ◽  
XiangYang Hou ◽  
Xiao Wang ◽  
...  
Keyword(s):  
Thermogravimetric Analysis ◽  
Benzoic Acid ◽  
Coordination Polymers ◽  
Layer Structure ◽  
Stacking Interactions ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
D10 Metal ◽  
Metal Coordination Polymers

AbstractTwo new coordination polymers (CPs), [Zn(npba)2] (1) and [Cd(npba)2] (2), have been hydrothermally synthesized from Zn(NO3)2·6H2O/Cd(NO3)2·6H2O and 3-nitro-5-(pyridin-3-yl) benzoic acid (Hnpba). The products have been characterized by IR spectroscopy, elemental analysis, thermogravimetric analysis, and single-crystal X-ray diffraction. In CP 1, the four-coordinated Zn(II) centers are bridged by npba ligands to generate chains, which are connected through arene π–π stacking interactions to generate a layer structure. In CP 2, the six-coordinated Cd(II) centers are also bridged by npba ligands to form chains with similar connectivity. The photoluminescence properties of CPs 1 and 2 were studied.

scholarly journals Crystal Engineering of Schiff Base Zn(II) and Cd(II) Homo- and Zn(II)M(II) (M = Mn or Cd) Heterometallic Coordination Polymers and Their Ability to Accommodate Solvent Guest Molecules

Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2317
Author(s):  
Olga Danilescu ◽  
Paulina N. Bourosh ◽  
Oleg Petuhov ◽  
Olga V. Kulikova ◽  
Ion Bulhac ◽  
...  
Keyword(s):  
Schiff Base ◽  
Coordination Polymers ◽  
Crystal Engineering ◽  
Self Assembly ◽  
X Ray Diffraction ◽  
Guest Molecules ◽  
X Ray ◽  
1D Chain ◽  
Two Temperatures ◽  
Adsorption Desorption

Based on solvothermal synthesis, self-assembly of the heptadentate 2,6-diacetylpyridine bis(nicotinoylhydrazone) Schiff base ligand (H2L) and Zn(II) and/or Cd(II) salts has led to the formation of three homometallic [CdL]n (1), {[CdL]∙0.5dmf∙H2O}n (2) and {[ZnL]∙0.5dmf∙1.5H2O}n (3), as well as two heterometallic {[Zn0.75Cd1.25L2]∙dmf∙0.5H2O}n (4) and {[MnZnL2]∙dmf∙3H2O}n coordination polymers. Compound 1 represents a 1D chain, whereas 2–5 are isostructural and isomorphous two-dimensional structures. The entire series was characterized by IR spectroscopy, thermogravimetric analysis, single-crystal X-ray diffraction and emission measurements. 2D coordination polymers accommodate water and dmf molecules in their cage-shaped interlayer spaces, which are released when the samples are heated. Thus, three solvated crystals were degassed at two temperatures and their photoluminescent and adsorption–desorption properties were recorded in order to validate this assumption. Solvent-free samples reveal an increase in volume pore, adsorption specific surface area and photoluminescence with regard to synthesized crystals.

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