The Synthesis and Structural Characterization of a Two-Dimensional Coordination Polymer [Co(H2O)(phen)(μ4-bta)1/2]n (H4bta = Benzenetetracarboxylic Acid)

2001 ◽  
Vol 66 (6) ◽  
pp. 870-876 ◽  
Author(s):  
De-Qing Chu ◽  
Ji-Qing Xu ◽  
Ao-Qing Tang
Keyword(s):  
Coordination Polymer ◽  
Single Crystal ◽  
Structural Characterization ◽  
Two Dimensional ◽  
Polymeric Structure ◽  
X Ray ◽  
X Ray Crystallography

Complex [Co(H2O)(phen)(μ4-bta)1/2]n was hydrothermally synthesized from sodium benzene-1,2,4,5-tetracarboxylate, 1,10-phenanthroline and CoCl2·6H2O, and structurally characterized by single-crystal X-ray crystallography, showing that it possesses a novel two-dimensional polymeric structure.

Synthesis and Structural Characterization of a New Two-Dimensional Polymeric Thallium(I) Complex, [Tl2(phthalate)]n

2005 ◽  
Vol 60 (7) ◽  
pp. 741-744 ◽  
Author(s):  
M. R. Fadaei ◽  
A. Morsali ◽  
Ali R. Mahjoub
Keyword(s):  
Coordination Polymer ◽  
Structural Characterization ◽  
Two Dimensional ◽  
X Ray ◽  
X Ray Crystallography

Determination of the structure of the [Tl2(phthalate)] by X-ray crystallography shows that there are six (TlO6) and five (TlO5) coordinate Tl atoms. The complex is a two-dimensional coordination polymer.

Synthesis and structural characterization of a magnesium phthalocyanine(3–) anion

2012 ◽  
Vol 16 (01) ◽  
pp. 154-162 ◽  
Author(s):  
Edwin W.Y. Wong ◽  
Daniel B. Leznoff
Keyword(s):  
Absorption Spectrum ◽  
Solid State ◽  
Single Crystal ◽  
Structural Characterization ◽  
Heterometallic Complex ◽  
State Structure ◽  
Solid State Structure ◽  
X Ray ◽  
X Ray Crystallography

The reduction of magnesium phthalocyanine (MgPc) with 2.2 equivalents of potassium graphite in 1,2-dimethoxyethane (DME) gives [K2(DME)4]PcMg(OH)(1) in 67% yield. Compound 1 was structurally characterized using single crystal X-ray crystallography and was found to be a monomeric, heterometallic complex consisting of a μ3-OH ligand that bridges a [MgIIPc3-]- anion to two potassium cations solvated by four DME molecules. An absorption spectrum of 1 confirms the Pc ligand is singly reduced and has a 3–charge. The solid-state structure of 1 does not indicate breaking of the aromaticity of the Pc ligand. Compound 1 is only the second Pc3- complex and the first reduced MgPc to be isolated and structurally characterized.

Tuning of crystallization method and ligand conformation to give a mononuclear compound or two-dimensional SCO coordination polymer based on a new semi-rigid V-shaped bis-pyridyl bis-amide ligand

2020 ◽  
Vol 76 (5) ◽  
pp. 412-418
Author(s):  
Xiaoyun Hao ◽  
Yong Dou ◽  
Tong Cao ◽  
Lan Qin ◽  
Lu Yang ◽  
...  
Keyword(s):  
Coordination Polymer ◽  
Single Crystal ◽  
Rational Design ◽  
High Spin State ◽  
Structure Type ◽  
Two Dimensional ◽  
Thermally Induced ◽  
X Ray ◽  
X Ray Crystallography ◽  
Ligand Conformation

With the new semi-rigid V-shaped bidentate pyridyl amide compound 5-methyl-N,N′-bis(pyridin-4-yl)benzene-1,3-dicarboxamide (L) as an auxiliary ligand and the FeII ion as the metal centre, one mononuclear complex, bis(methanol-κO)bis[5-methyl-N,N′-bis(pyridin-4-yl)benzene-1,3-dicarboxamide-κN]bis(thiocyanato-κN)iron(II), [Fe(SCN)2(C19H16N4O2)2(CH3OH)2] (1), and one two-dimensional coordination polymer, catena-poly[[[bis(thiocyanato-κN)iron(II)]-bis[μ-5-methyl-N,N′-bis(pyridin-4-yl)benzene-1,3-dicarboxamide-κ2 N:N′]] methanol disolvate dihydrate], {[Fe(SCN)2(C19H16N4O2)2]·2CH3OH·2H2O} n (2), were prepared by slow evaporation and H-tube diffusion methods, respectively, indicating the effect of the method of crystallization on the structure type of the target product. Both complexes have been structurally characterized by elemental analysis, IR spectroscopy and single-crystal X-ray crystallography. The single-crystal X-ray diffraction analysis shows that L functions as a monodentate ligand in mononuclear 1, while it coordinates in a bidentate manner to two independent Fe(SCN)2 units in complex 2, with a different conformation from that in 1 and the ligands point in two almost orthogonal directions, therefore leading to a two-dimensional grid-like network. Investigation of the magnetic properties reveals the always high-spin state of the FeII centre over the whole temperature range in 1 and a gradual thermally-induced incomplete spin crossover (SCO) behaviour below 150 K in 2, demonstrating the influence of the different coordination fields on the spin properties of the metal ions. The current results provide useful information for the rational design of functional complexes with different structure dimensionalities by employing different conformations of the ligand and different crystallization methods.

Methane Sorption and Structural Characterization of the Sorption Sites in Zn2(bdc)2(dabco) by Single Crystal X-ray Crystallography

2009 ◽  
Vol 4 (6) ◽  
pp. 886-891 ◽  
Author(s):  
Hyunuk Kim ◽  
Denis G. Samsonenko ◽  
Sunirban Das ◽  
Ghyung-Hwa Kim ◽  
Heung-Soo Lee ◽  
...  
Keyword(s):  
Single Crystal ◽  
Structural Characterization ◽  
X Ray ◽  
X Ray Crystallography ◽  
Methane Sorption

Synthesis and structural characterization of a Ni(II) coordination polymer with a tripodal 4-imidazolyl-functional ligand

2019 ◽  
Vol 74 (11-12) ◽  
pp. 857-860
Author(s):  
Hai-Wei Kuai ◽  
Xiao-Hong Zhu ◽  
Ding-Yun Jiang ◽  
Xiao-Chun Cheng ◽  
Deng-Hao Li
Keyword(s):  
Infrared Spectroscopy ◽  
Coordination Polymer ◽  
Single Crystal ◽  
Network Structure ◽  
Structural Characterization ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray

Abstract1,3,5-Tri(1H-imidazol-4-yl)benzene (H3L) reacts with Ni(ClO4)2 · 6H2O under hydrothermal conditions at T = 100°C to yield a new complex: [Ni(H2L)2] · 5.5H2O (1). The product is characterized by single crystal and powder X-ray diffraction, infrared spectroscopy, and elemental and thermogravimetric analyses. Complex 1 crystallizes in the monoclinic space group C2/c and exhibits a binodal (3,6)-connected 2D kgd network structure with (43)2(46.66.83) topology.

Structural characterization of (±)-3-aryl-1-azabicyclo[2.2.2]octan-3-ols by two-dimensional NMR spectroscopy and X-Ray crystallography. I

1991 ◽  
Vol 29 (11) ◽  
pp. 1130-1139 ◽  
Author(s):  
M. S. Arias-Pérez ◽  
A. Cosme ◽  
E. Gálvez ◽  
F. Florencio ◽  
I. Fonseca ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Structural Characterization ◽  
Two Dimensional ◽  
X Ray ◽  
X Ray Crystallography

scholarly journals Structural Characterization of Heterodinuclear ZnII-LnIII Complexes (Ln = Pr, Nd) with a Ring-Contracted H2valdien-Derived Schiff Base Ligand

2021 ◽  
Author(s):  
Shabana Noor ◽  
Richard Goddard ◽  
Fehmeeda Khatoon ◽  
Sarvendra Kumar ◽  
Rüdiger W. Seidel
Keyword(s):  
Molecular Structure ◽  
Schiff Base ◽  
Structural Characterization ◽  
Schiff Base Ligand ◽  
Crystal And Molecular Structure ◽  
X Ray ◽  
X Ray Crystallography ◽  
Imidazoline Ring

AbstractSynthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes with the formula [ZnLn(HL)(µ-OAc)(NO3)2(H2O)x(MeOH)1-x]NO3 · n H2O · n MeOH [Ln = Pr (1), Nd (2)] and the crystal and molecular structure of [ZnNd(HL)(µ-OAc)(NO3)2(H2O)] [ZnNd(HL)(OAc)(NO3)2(H2O)](NO3)2 · n H2O · n MeOH (3) are reported. The asymmetrical compartmental ligand (E)-2-(1-(2-((2-hydroxy-3-methoxybenzylidene)amino)-ethyl)imidazolidin-2-yl)-6-methoxyphenol (H2L) is formed from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation, resulting in a peripheral imidazoline ring. The structures of 1–3 were revealed by X-ray crystallography. The smaller ZnII ion occupies the inner N2O2 compartment of the ligand, whereas the larger and more oxophilic LnIII ions are found in the outer O2O2’ site. Graphic Abstract Synthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes (Ln = Pr, Nd) bearing an asymmetrical compartmental ligand formed in situ from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation are reported.

Structural Systematics of Rare Earth Complexes. VII. Crystal Structure of Bis(2,2'/6',2␛-Terpyridinium) Octaaquaterbium(III) Heptachloride Hydrate

1994 ◽  
Vol 47 (2) ◽  
pp. 391 ◽  
Author(s):  
CJ Kepert ◽  
BW Skeleton ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Rare Earth ◽  
Single Crystal ◽  
Structural Characterization ◽  
Title Compound ◽  
Room Temperature ◽  
Chloride Ions ◽  
Full Matrix ◽  
X Ray

The room-temperature single-crystal X-ray structural characterization of the title compound (tpyH2)2[Tb(OH2)8]Cl7.~2⅓H2O is recorded. Crystals are triclinic, Pī , a 17.063(5), b 16.243(3), c 7.878(3) Ǻ, α 84.78(2), β 84.39(3), γ 87.81(2)°, Z = 2 formula units; 3167 'observed' diffractometer reflections were refined by full-matrix least-squares procedures to a residual of 0.057. Notable features of interest of the compound are the 'chelation' of chloride ions by the terpyridinium cations , and the existence of a free [Tb(OH2)8]2+ cation in the presence of an abundance of chloride ions.

scholarly journals The Synthesis and Characterization of a Novel One-Dimensional Bismuth (III) Coordination Polymer as a Precursor for the Production of Bismuth (III) Oxide Nanorods

Crystals ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 113
Author(s):  
Younes Hanifehpour ◽  
Babak Mirtamizdoust ◽  
Jaber Dadashi ◽  
Ruiyao Wang ◽  
Mahboube Rezaei ◽  
...  
Keyword(s):  
Single Crystal ◽  
Coordination Compound ◽  
Organic Ligand ◽  
One Dimensional ◽  
X Ray ◽  
X Ray Crystallography ◽  
Oxide Nanorods ◽  
Pure Phase ◽  
3D Framework

A novel Bi (III) coordination compound, [Bi(HQ)(Cl)4]n ((Q = pyridine-4-carbaldehyde thiosemicarbazone), was prepared in this research using a sonochemical technique. SEM, infrared spectroscopy (IR), XRD, and single-crystal X-ray analysis were utilized to analyze the Bi(III) coordination compound. The structure determined using single-crystal X-ray crystallography indicates that the coordination compound is a 1D polymer in solid state and that the coordination number of bismuth (III) ions is six, (BiSCl5), with one S donor from the organic ligand and five Cl donors from anions. It is equipped with a hemidirectional coordination sphere. It is interesting that the ligand has been protonated in the course of the reaction with a Cl- ion balancing the charge. This compound’s supramolecular properties are directed and regulated by weak directional intermolecular interactions. Through π–π stacking interactions, the chains interact with one another, forming a 3D framework. Thermolysis of the compound at 170 °C with oleic acid resulted in the formation of pure phase nanosized Bi (III) oxide. SEM technique was used to examine the morphology and size of the bismuth (III) oxide product produced.

scholarly journals Structural characterization of alloxazine and substituted isoalloxazines: NMR and X-ray crystallography

ARKIVOC ◽  
2006 ◽  
Vol 2007 (4) ◽  
pp. 20-38 ◽  
Author(s):  
Mª Ángeles Farrán ◽  
Rosa Mª Claramunt ◽  
Concepción López ◽  
Elena Pinilla ◽  
Mª Rosario Torres ◽  
...  
Keyword(s):  
Structural Characterization ◽  
X Ray ◽  
X Ray Crystallography
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