Syntheses, spectroscopic study and X-ray crystallography of some new phosphoramidates and lanthanide(III) complexes of N-(4-nitrobenzoyl)-N′,N′′-bis(morpholino)phosphoric triamide

2010 ◽  
Vol 66 (4) ◽  
pp. 441-450 ◽  
Author(s):  
Khodayar Gholivand ◽  
Hossein Mostaanzadeh ◽  
Tomas Koval ◽  
Michal Dusek ◽  
Mauricio F. Erben ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Ir Spectroscopy ◽  
Elemental Analysis ◽  
Quantum Chemical ◽  
Free Ligand ◽  
Conformational Behavior ◽  
Neutral Ligand ◽  
X Ray ◽  
X Ray Crystallography ◽  
Phosphoric Triamide

New phosphoramidates with the formula RC(O)N(H)P(O)X 2, R = 2-NO2—C6H4, 3-NO2—C6H4 and 4-NO2—C6H4, X = N(CH2CH3) (1)–(3), NC4H8 (4)–(6), and NC4H8O (7)–(9) were synthesized and characterized by 1H, 13C, 31P NMR and IR spectroscopy, and elemental analysis. The reaction of (9) with hydrated lanthanide(III) nitrate leads to ten- or nine-coordinated complexes, (10)–(13). The crystal structure has been determined for (3), (5), (9), (10) and (13). In contrast to all of the previously reported similar phosphoramidate compounds, the —C(O)—N(H)—P(O) skeleton in the free ligand (9) shows a cisoid conformation, with the C=O and P=O double bonds adopting a nearly syn conformation. Quantum chemical calculations were applied for clarifying this exceptional conformational behavior. The monodentate neutral ligand (9) is coordinated to the metal ions via the phosphoryl O atom, adopting the usual anti conformation between the C=O and P=O groups.

scholarly journals Crystal structure of an oxalate-bridged tetranuclear 8-hydroxyquinoline Zn(II) cluster: [Zn4Q6(Ox)]0.5n

2011 ◽  
Vol 76 (4) ◽  
pp. 529-537 ◽  
Author(s):  
Jiajun Wang ◽  
Qiang Wang ◽  
Yanjun Sun ◽  
Yuemei Wang ◽  
Guosheng Zhao ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Thermal Analysis ◽  
Ir Spectroscopy ◽  
Elemental Analysis ◽  
Chain Structure ◽  
Stacking Interactions ◽  
Monoclinic System ◽  
X Ray ◽  
X Ray Crystallography ◽  
Polymeric Chains

The chain structure of a tetranuclear zinc(II) cluster [Zn4Q6(Ox)]0.5n ([Zn4 (C9H6NO)6(C2O4)]0.5n) (1) (Q = 8- hydroxyquinoline anion, Ox = oxalate dianion) was determined by X-ray crystallography and characterized by elemental analysis, IR spectroscopy and thermal analysis. It crystallizes in the monoclinic system, space group P21/n (No. 14), with the lattice parameters a = 13.2222(15) ?, b = 11.0566(12) ?, c = 16.2224(18) ?, ? = 92.1770(10)?, V = 2369.9(5) ?3, Z = 4, Mr = 607.23 g mol-1, Dc = 1.702 g cm-3. The tetranuclear zinc(II) clusters form 1D polymeric chains parallel to the b-axis. The ?-? stacking interactions involving aryl rings support the formation of the 1D polymeric structure. The neighboring polymeric chains are connected by C-H???? interactions.

Hydrothermal Synthesis, Crystal Structure and Properties of a Novel 3D Metal-Organic Cd(II) Coordination Polymer Based on Helical Units

2013 ◽  
Vol 68 (2) ◽  
pp. 127-132
Author(s):  
Hai-Hua Li ◽  
Peng Zhang ◽  
Jia-Yi Pu ◽  
Yu-Ying Zhao ◽  
Chong-Zhen Mei
Keyword(s):  
Crystal Structure ◽  
Hydrothermal Synthesis ◽  
Ir Spectroscopy ◽  
Coordination Polymer ◽  
Elemental Analysis ◽  
Metal Organic Framework ◽  
Structure And Properties ◽  
X Ray ◽  
X Ray Crystallography ◽  
Metal Organic

A metal-organic framework based on 4-methylphthalic acid (H2L) and 4,4’-bipyridine (bpy), namely {[Cd(L)(bpy)1:5]·2(H2O)}n (1), has been synthesized hydrothermally and characterized by IR spectroscopy, elemental analysis, thermogravimetry, and single-crystal X-ray crystallography. Complex 1 exhibits a 3D coordination network based on layers. Each layer consists of left- or right-handed {Cd-L-Cd-bpy-Cd-L-Cd-bpy}n double helices.Water molecules are also incorporated in the network. Compound 1 shows fluorescence at ca. 360 nm upon excitation at 304 nm.

A Zinc(II)-Silver(I) Bimetallic Coordination Polymer Assembled Through Argentophilic and π-π Interactions, f[Zn(phen)2(H2O) {Ag(CN)2g][Ag(CN)2]·MeOH}n (phen=1,10-Phenanthroline)

2013 ◽  
Vol 68 (2) ◽  
pp. 161-167 ◽  
Author(s):  
Muhammad Monim-ul-Mehbooba ◽  
Muhammad Ramzan ◽  
Tobias Rüffe ◽  
Heinrich Lang ◽  
Shafqat Naddem ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Thermal Analysis ◽  
Ir Spectroscopy ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
X Ray ◽  
Π Interactions ◽  
X Ray Crystallography ◽  
3D Network ◽  
Argentophilic Interactions

A cyanido-bridged Zn(II)-Ag(I) bimetallic coordination polymer, {[Zn(phen)2(H2O){Ag(CN)2}] [Ag(CN)2]·MeOH}n (1), was prepared using ZnCl2, 1,10-phenanthroline (phen) and K[Ag(CN)2] and characterized by IR spectroscopy, thermal analysis and X-ray crystallography. The crystal structure of 1 consists of dinuclear [Zn(phen)2(H2O){Ag(CN)2}]+ cations, [Ag(CN)2]- anions and a methanol molecule. The non-coordinated [Ag(CN)2]- anions are linked to the [Zn(phen)2(H2O){Ag(CN)2}]+ complex cations through argentophilic interactions leading to the formation of chains. The chains are connected by hydrogen bonds and π-π interactions to give a 3D network.

Synthesis, characterization, crystal structure, electrochemical, solvatochromic and biological investigation of novel N4 and N3 type Cu(ii) Schiff base complexes

2017 ◽  
Vol 41 (21) ◽  
pp. 12554-12561 ◽  
Author(s):  
Akbar Azary ◽  
Abolfazl Bezaatpour ◽  
Saber Zahri ◽  
Mandana Amiri
Keyword(s):  
Crystal Structure ◽  
Schiff Base ◽  
Infrared Spectroscopy ◽  
Elemental Analysis ◽  
Schiff Base Complexes ◽  
Conductivity Measurements ◽  
Biological Investigation ◽  
X Ray ◽  
X Ray Crystallography

In the present study, three novel Cu(ii) Schiff base complexes were synthesized and characterized using infrared spectroscopy, elemental analysis, conductivity measurements and X-ray crystallography.

scholarly journals Synthesis and Characterisation of Zinc(II) Complex With 2-Amino-5-bromopyridine Ligand

2017 ◽  
Author(s):  
Fitriani
Keyword(s):  
Ir Spectroscopy ◽  
Elemental Analysis ◽  
Coordination Geometry ◽  
Tetrahedral Coordination ◽  
Visible Absorption ◽  
X Ray ◽  
X Ray Crystallography ◽  
Uv Visible ◽  
Cl Atoms ◽  
Distorted Tetrahedral Coordination

The synthesis and characterisation of zinc(II) complex with 2-amino-5-bromopyridine (C5H5BrN2) ligand have been described. The complex was structurally characterised via X-ray crystallography, in the title compound, (2-amino-5-bromopyridinium) [ZnCl¬3(2-amino-5-bromopyridine)] or which is also called (C5H6BrN2) [ZnCl3(C5H5BrN2)]¬. The Zn(II) atom is four-coordinated by three Cl atoms and one imine N-atom of 2-amino-5-bromopyridine ligand, forming a distorted tetrahedral coordination geometry. The complex was also investigated by elemental analysis, 1H NMR, IR spectroscopy and UV-Visible absorption. The protonation behaviour upon coordination is discussed.

A Three-Dimensional Silver(I) Framework Assembled from Nitrilotriacetate

2005 ◽  
Vol 58 (2) ◽  
pp. 115 ◽  
Author(s):  
Chun-Long Chen ◽  
Qian Zhang ◽  
Ji-Jun Jiang ◽  
Qin Wang ◽  
Cheng-Yong Su
Keyword(s):  
Crystal Structure ◽  
Ir Spectroscopy ◽  
Coordination Polymer ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Three Dimensional ◽  
Single Crystal Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Coordination Numbers

The reaction of AgCF3CO2 with nitrilotriacetate (NTA) yields the three-dimensional silver(i) coordination polymer {Ag3[N(CH2COO)3]}n 1 which was characterized by means of elemental analysis and IR spectroscopy as well as X-ray diffraction. The single crystal structure shows that the NTA3– anions act as unusual heptadentate 13-coordination agents and the silver(i) atoms exhibit various coordination numbers in the range 3–6.

A new modification of [Ag4Br4(PPh3)4]: synthesis, structure and properties

2018 ◽  
Vol 73 (10) ◽  
pp. 733-738 ◽  
Author(s):  
Xintong Han ◽  
Shanshan Mao ◽  
Chuang Li ◽  
Kesheng Shen ◽  
Xinkui Shi ◽  
...  
Keyword(s):  
Solid State ◽  
Ir Spectroscopy ◽  
Hydrogen Bonds ◽  
Elemental Analysis ◽  
Supramolecular Structure ◽  
Chair Conformation ◽  
Cyclic Voltammograms ◽  
Structure And Properties ◽  
X Ray ◽  
X Ray Crystallography

AbstractA new modification of the homometallic silver(I) cluster [Ag4Br4(PPh3)4] has been prepared and characterized by elemental analysis, UV/Vis and IR spectroscopy, and X-ray crystallography. The tetramer shows a polycyclic structure with a chair conformation. The bromine atoms adopt μ2- and μ3-bridging modes. The shortest Ag–Ag distance in the cluster is 3.159(2) Å, which indicates significant Ag–Ag interactions. A supramolecular structure is arranged by hydrogen bonds (C–H···Br). Cyclic voltammograms of the cluster indicate a quasi-reversible Ag+/Ag couple. The fluorescence properties of the ligand and the Ag(I) cluster were studied in the solid state. The emission peaks of the Ag(I) cluster are attributed to ligand-centered luminescence.

Retention of (4,4) Connectivity in the Absence of π…π Interactions in a Cadmium tris-Dicyanamide Compound

2006 ◽  
Vol 59 (2) ◽  
pp. 115 ◽  
Author(s):  
Moumita Biswas ◽  
Stuart R. Batten ◽  
Paul Jensen ◽  
Samiran Mitra
Keyword(s):  
Thermogravimetric Analysis ◽  
Ir Spectroscopy ◽  
Powder Diffraction ◽  
Elemental Analysis ◽  
Octahedral Geometry ◽  
X Ray ◽  
Π Interactions ◽  
X Ray Crystallography ◽  
Extended Sheets

An anionic cadmium tris-dicyanamide compound (Et4N)[Cd(N(CN)2)3]·3/4H2O 1 has been synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis, X-ray powder diffraction, and X-ray crystallography. The anions form extended sheets with retention of (4,4) connectivity in the absence of π···π interactions within the cation layers, and with octahedral geometry about individual CdII ions.

Preparation and Characterization of Macrocyclic Dinickel Complexes Coligated by Tetrazolate Ligands

2008 ◽  
Vol 63 (5) ◽  
pp. 496-502 ◽  
Author(s):  
Vasile Lozan ◽  
Sergei V. Voitekhovich ◽  
Pavel N. Gaponik ◽  
Oleg A. Ivashkevich ◽  
Berthold Kersting
Keyword(s):  
Ir Spectroscopy ◽  
Elemental Analysis ◽  
X Ray ◽  
X Ray Crystallography

The dinuclear nickel(II) complex [Ni2LCl]+ (1), where (L)2− represents a 24-membered macrocyclic hexamine-dithiophenolate ligand, reacts readily with 5-R-tetrazolate ligands to give the complexes [Ni2L(RCN4)]+, where R = H (2), Me (3), Ph (4). The new complexes were either isolated as perchlorate or tetraphenylborate salts and fully characterized by elemental analysis, UV/Vis, and IR spectroscopy. The structures of 2[BPh4] · MeCN, 3[BPh4] · 2MeCN, and 4[BPh4] ·MeCN were determined by X-ray crystallography, showing that all tetrazolate units are in a 2,3-bridging mode to generate dioctahedral N3Ni(μ-S)2(μ-N4CR)NiN3 core structures. The RCN4− groups interact less strongly with the [Ni2L]2+ fragment than pyrazolate ligands (CH)3N2 − as reflected in the longer Ni-N distances.

Syntheses and Spectroscopic Studies of Some New Diazaphospholes and Diazaphosphorinanes. Crystal Structure of 4

2005 ◽  
Vol 60 (10) ◽  
pp. 1021-1026 ◽  
Author(s):  
Khodayar Gholivand ◽  
Zahra Shariatinia ◽  
Mehrdad Pourayoubi ◽  
Sedigheh Farshadian
Keyword(s):  
Crystal Structure ◽  
Ir Spectroscopy ◽  
Spectroscopic Studies ◽  
Coupling Constants ◽  
Crystalline Lattice ◽  
Polymeric Chain ◽  
Ring Strain ◽  
One Dimensional ◽  
X Ray ◽  
X Ray Crystallography

New diazaphospholes and diazaphosphorinanes with formula were synthesized and characterized by 1H, 13C, 31P NMR and IR spectroscopy and elemental analysis. The structure of compound 1 has been determined by X-ray crystallography. A one-dimensional polymeric chain was observed in the crystalline lattice produced by intermolecular -P=O. . .H-N- and -C=O. . .H-N-hydrogen bonds. Compounds 1 and 2 contain five-membered rings and show high values for 2J(PNH) and 2J(P,C) coupling constants due to the ring strain. These constants are reduced seriously in compounds with six-membered rings. In compound 6 with CCl3C(O)NH moiety, all phosphorus-hydrogen couplings are zero.

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