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1.
Metal(II) Ion Complexes with 5‐(Pyrazin‐2‐yl)‐2,4‐dihydro‐3H‐1,2,4‐triazole‐3‐thione; Synthesis,Structural Characterization,Acid‐base,and Complexing Properties in Solution 下载免费PDF全文
Aleksander Kufelnicki Jolanta Jaciubek‐Rosińska Marta Sobiesiak Agata Paneth Julia Jezierska Elzbieta Budzisz 《无机化学与普通化学杂志》2017,643(16):1067-1074
The study reports the synthesis of complexes Co(HL)Cl2 ( 1 ), Ni(HL)Cl2 ( 2 ), Cu(HL)Cl2 ( 3 ), and Zn(HL)3Cl2 ( 4 ) with the title ligand, 5‐(pyrazin‐2‐yl)‐1,2,4‐triazole‐5‐thione (HL), and their characterization by elemental analyses, ESI‐MS (m/z), FT‐IR and UV/Vis spectroscopy, as well as EPR in the case of the CuII complex. The comparative analysis of IR spectra of the metal ion complexes with HL and HL alone indicated that the metal ions in 1 , 2 , and 3 are chelated by two nitrogen atoms, N(4) of pyrazine and N(5) of triazole in the thiol tautomeric form, whereas the ZnII ion in 4 is coordinated by the non‐protonated N(2) nitrogen atom of triazole in the thione form. pH potentiometry and UV/Vis spectroscopy were used to examine CoII, NiII, and ZnII complexes in 10/90 (v/v) DMSO/water solution, whereas the CuII complex was examined in 40/60 (v/v) DMSO/water solution. Monodeprotonation of the thione triazole in solution enables the formation of the L:M = 1:1 species with CoII, NiII and ZnII, the 2:1 species with CoII and ZnII, and the 3:1 species with ZnII. A distorted tetrahedral arrangement of the CuII complex was suggested on the basis of EPR and Vis/NIR spectra. 相似文献
2.
Yasunori Muranishi Yue Wang Mamiko Odoko Nobuo Okabe 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(6):m307-m310
In the three title complexes, namely (2,2′‐biquinoline‐κ2N,N′)dichloropalladium(II), [PdCl2(C18H12N2)], (I), and the corresponding copper(II), [CuCl2(C18H12N2)], (II), and zinc(II) complexes, [ZnCl2(C18H12N2)], (III), each metal atom is four‐coordinate and bonded by two N atoms of a 2,2′‐biquinoline molecule and two Cl atoms. The PdII atom has a distorted cis‐square‐planar coordination geometry, whereas the CuII and ZnII atoms both have a distorted tetrahedral geometry. The dihedral angles between the N—M—N and Cl—M—Cl planes are 14.53 (13), 65.42 (15) and 85.19 (9)° for (I), (II) and (III), respectively. The structure of (II) has twofold imposed symmetry. 相似文献
3.
Mariana Dennehy Oscar V. Quinzani Ricardo Faccio Eleonora Freire lvaro W. Mombrú 《Acta Crystallographica. Section C, Structural Chemistry》2012,68(1):m12-m16
(Acetonitrile‐1κN)[μ‐1H‐benzimidazole‐2(3H)‐thione‐1:2κ2S:S][1H‐benzimidazole‐2(3H)‐thione‐2κS]bis(μ‐1,1‐dioxo‐1λ6,2‐benzothiazole‐3‐thiolato)‐1:2κ2S3:N;1:2κ2S3:S3‐dicopper(I)(Cu—Cu), [Cu2(C7H4NO2S2)2(C7H6N2S)2(CH3CN)] or [Cu2(tsac)2(Sbim)2(CH3CN)] [tsac is thiosaccharinate and Sbim is 1H‐benzimidazole‐2(3H)‐thione], (I), is a new copper(I) compound that consists of a triply bridged dinuclear Cu—Cu unit. In the complex molecule, two tsac anions and one neutral Sbim ligand bind the metals. One anion bridges via the endocyclic N and exocyclic S atoms (μ‐S:N). The other anion and one of the mercaptobenzimidazole molecules bridge the metals through their exocyclic S atoms (μ‐S:S). The second Sbim ligand coordinates in a monodentate fashion (κS) to one Cu atom, while an acetonitrile molecule coordinates to the other Cu atom. The CuI—CuI distance [2.6286 (6) Å] can be considered a strong `cuprophilic' interaction. In the case of [μ‐1H‐benzimidazole‐2(3H)‐thione‐1:2κ2S:S]bis[1H‐benzimidazole‐2(3H)‐thione]‐1κS;2κS‐bis(μ‐1,1‐dioxo‐1λ6,2‐benzothiazole‐3‐thiolato)‐1:2κ2S3:N;1:2κ2S3:S3‐dicopper(I)(Cu—Cu), [Cu2(C7H4NO2S2)2(C7H6N2S)3] or [Cu2(tsac)2(Sbim)3], (II), the acetonitrile molecule is substituted by an additional Sbim ligand, which binds one Cu atom via the exocylic S atom. In this case, the CuI—CuI distance is 2.6068 (11) Å. 相似文献
4.
Julio Gutierrez Rodney Eisenberg Gabrielle Herrensmith Thomas Tobin Tonglei Li Sihui Long 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(8):o310-o314
The structures of orthorhombic (E)‐4‐(2‐{[amino(iminio)methyl]amino}vinyl)‐3,5‐dichlorophenolate dihydrate, C8H8Cl2N4O·2H2O, (I), triclinic (E)‐4‐(2‐{[amino(iminio)methyl]amino}vinyl)‐3,5‐dichlorophenolate methanol disolvate, C8H8Cl2N4O·2CH4O, (II), and orthorhombic (E)‐amino[(2,6‐dichloro‐4‐hydroxystyryl)amino]methaniminium acetate, C8H9Cl2N4O+·C2H3O2−, (III), all crystallize with one formula unit in the asymmetric unit, with the molecule in an E configuration and the phenol H atom transferred to the guanidine N atom. Although the molecules of the title compounds form extended chains via hydrogen bonding in all three forms, owing to the presence of different solvent molecules, those chains are connected differently in the individual forms. In (II), the molecules are all coplanar, while in (I) and (III), adjacent molecules are tilted relative to one another to varying degrees. Also, because of the variation in hydrogen‐bond‐formation ability of the solvents, the hydrogen‐bonding arrangements vary in the three forms. 相似文献
5.
S. Ahmad T. Rüffer H. Lang S. Nadeem S. A. Tirmizi M. Saleem A. Anwar 《Russian Journal of Coordination Chemistry》2010,36(7):520-524
The palladium(II) complex, [Pd(PPh3)2(Imt)2]Cl2 · 3.5H2O (I) (Imt = imidazolidine-2-thione), has been synthesized and characterized by IR, NMR, and X-ray crystallography. An upfield
shift in the >C=S resonance of Imt in the 13C NMR spectrum and a downfield shift in the N-H resonance in 1H NMR are consistent with the sulfur coordination of Imt to palladium(II). In the crystal structure of I, the central palladium atom is coordinated to two thione sulfur atoms of Imt and to two phosphorus atoms possessing a square-planar
environment with the average cis and trans bond angles of 89.60° and 167.31°, respectively. The title complex was screened for antimicrobial effects, and the results
showed that it exhibits moderate activities against gram-negative bacteria (E. coli, P. aeruginosa). The complexes also exhibited significant activities against yeast (C. albicans, S. serevisaiae). 相似文献
6.
121Sb Mössbauer Spectra. IV. Benzamidine Complexes of Antimony(V). Crystal Structure of [Ph2Cl2Sb(N2Me2CPh)] The 121Sb Mössbauer spectra of the octahedral benzamidine complexes [Cl4Sb[BAN)]] ( I ), [Ph2Cl3Sb(BAN)] ( II ), [Ph2Cl2Sb(BAN)] ( III ), and [Ph3ClSb(BAN)] ( IV ) (BAN = N,N′-dimethyl-benzamidine) were measured at 4.2 K. The configuration of the complexes II–IV is derived from the values of the quadrupol split. In II the phenyl group is arranged in the axis, III contains both phenyl groups in equatorial position, located in trans-position to the N atoms of the chelate ligand, whereas in IV one phenyl group is placed axially, the other two are in equatorial position. The measurements are supplemented by the vibrational spectra below 600 cm?1. Complex III crystallizes in the monoclinic space group P21/c with four formula units per unit cell. In addition, four molecules of CCl4 per unit cell are placed in cavities of the lattice. The refinement has been carried on to an R-value of 6.5%, taking into account 1 729 unique, observed reflexions. The structure consists of discrete molecules of [Ph2Cl2Sb(N2Me2CPh)], in which the antimony atoms are surrounded by the N atoms of the chelate ligand, the phenyl groups and the two axial Cl atoms in distorted octahedral arrangement. The planes of the phenyl rings form dihedral angles with the equatorial plane of 129° and 143°. 相似文献
7.
Dubravka Matkovi‐alogovi Zora Popovi Gordana Pavlovi
eljka Soldin Gerald Giester 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(4):409-411
The reaction of 3,4,5,6‐tetrahydropyrimidine‐2‐thione (H4pymtH) with mercury(II) iodide in methanol in a 1:1 molar ratio resulted in the formation of single crystals of the title compound, [Hg(C4H8N2S)I2]. The Hg atom is coordinated by one S atom from H4pymtH at 2.456 (2) Å and by two I atoms at distances of 2.6872 (7) and 2.7044 (6) Å, and has a characteristic deformed trigonal coordination geometry. The molecule has crystallographic m symmetry but the Hg atom is disordered above and below the mirror plane. 相似文献
8.
Wolfgang Jeitschko Rainer O. Altmeyer Michael Schelk Ute Ch. Rodewald 《无机化学与普通化学杂志》2001,627(8):1932-1940
The title compounds are formed by peritectic reactions. Single crystals could be isolated from samples with high antimony content. Their structure was determined for Dy2Sb5 from four‐circle X‐ray diffractometer data: P21/m, a = 1306.6(1) pm, b = 416.27(4) pm, c = 1458.4(1) pm, β = 102.213(8)°, Z = 4, R = 0.061 for 2980 structure factors and 86 variable parameters. All dysprosium atoms have nine antimony neighbors forming tricapped trigonal prisms with Dy–Sb distances varying between 308 and 338 pm. The antimony atoms occupy ten different sites with greatly varying coordination. One extreme case is an antimony atom surrounded only by dysprosium atoms in trigonal prismatic arrangement, the other one is an antimony atom in distorted octahedral antimony coordination. The various antimony‐antimony interactions (with Sb–Sb distances varying between 284 and 338 pm) are rationalized by combining the Zintl‐Klemm concept with bond‐length bond‐strength considerations. 相似文献
9.
Bis(dimethylstibanyl)oxane ( 1 ) and ‐sulfane ( 2 ), the two simplest organoelement species with an Sb–E–Sb fragment (E = O, S), were prepared by alkaline hydrolysis of bromodimethylstibane and by oxidation of tetramethyldistibane with sulfur [18], respectively. As shown by an x‐ray structure analysis of compound 1 (m. p. < –20 °C; P212121, a = 675.9(2), b = 803.1(2), c = 1666.8(4) pm at –70 ± 2 °C; Z = 4; R1 = 0.042), the molecules (O–Sb 198.8 and 209.9 pm, Sb–O–Sb 123.0°) adopt a syn‐anti conformation in the solid state and are arranged in zigzag chains along [010] via weak intermolecular O‥Sb interactions (258.5 pm, Sb–O‥Sb 117.8°, O‥Sb–O 173.5°) making use, however, of only one Me2Sb moiety. Primary and secondary bond lengths and angles agree very well with corresponding values published for valentinite, the orthorhombic modification of antimony(III) oxide [3]. Bis(dimethylstibanyl)sulfane ( 2 ) (m. p. 29 to 31 °C) crystallizes in the uncommon space group P6522 (a = 927.8(3), c = 1940.9(7) pm at –100 ± 2 °C; Z = 6; R1 = 0.021). Owing to coordination numbers of (1 + 1) and (2 + 2) for both Me2Sb groups and the sulfur atom, respectively, molecules with an approximate syn‐syn conformation (S–Sb 249.8 pm, Sb–S–Sb 92.35°) build up a three‐dimensional net of double helices which are linked together by Sb‥S contacts (316.4 pm). These parameters shed more light onto the rather complicated structure and bonding situation in stibnite (antimony(III) sulfide [4]). The molecular packing of compound 2 is compared with the structures of relevant inorganic solids, especially with that of β‐quartz [37]. 相似文献
10.
By alternating‐current electrochemical technique crystals of copper(I) π‐complex with 1‐allylpyridinium chloride of [C5H5N(C3H5)][Cu2Cl3] ( 1 ) composition have been obtained and structurally investigated. Compound 1 crystallizes in monoclinic system, space group C2/c a = 24.035(1) Å, b = 11.4870(9) Å, c = 7.8170(5) Å, β = 95.010(5)°, V = 2150.0(2) Å3 (at 100 K), Z = 8, R = 0.028, for 4836 independent reflections. In the structure 1 trigonal‐pyramidal environment of π‐coordinated copper(I) atom is formed by a lengthened to 1.376(2) Å C=C bond of allyl group and by three chlorine atoms. Other two copper atoms are tetrahedrally surrounded by chlorine atoms only. The coordination polyhedra are combined into an original infinite (Cu4Cl62—)n fragment. Structural comparison of 1 and the recently studied copper(I) chloride π‐complexes with 3‐amino‐, 2‐amino‐, 4‐amino‐1‐allylpyridinium chlorides of respective [LCu2Cl3] ( 2 ), [L2Cu2Cl4] ( 3 ), and [LCuCl2] ( 4 ) compositions allowed us to reveal the trend of the inorganic fragment complication which depends on pKa (base) value of the corresponding initial heterocycle. 相似文献
11.
Oxidative Addition of N‐chlorotriphenylphosphoraneimine onto Phosphorus(III) Chloride and Antimony(III) Chloride. Crystal Structures of (Cl3PNPPh3)2[PCl6][ClHCl], [SbCl4(HNPPh3)2][SbCl6], and [Sb(NPPh3)4][SbCl6] Phosphorus(III) chloride reacts with N‐chlorotriphenylphosphoraneimine, ClNPPh3, in CH2Cl2 solution strongly exothermically via oxidative addition to give (Cl3PNPPh3)2[PCl6][ClHCl] ( 1 ). As a by‐product, Ph3PNP(O)Cl2 can be obtained, which is formed from PCl3 and ClNPPh3 in the presence of POCl3. In contrast to these results, antimony(III) chloride reacts with ClNPPh3 in CH2Cl2 solution to give a mixture of the phosphoraneimine complex [SbCl4(HNPPh3)2][SbCl6] ( 2 ) and the phosphoraneiminato complex [Sb(NPPh3)4][SbCl6] ( 3 ). The complexes 1 ‐ 3 were characterized by IR spectroscopy and by single crystal X‐ray determinations. 1 : Space group C2/c, Z = 4, lattice dimensions at 193 K: a = 3282.0(2), b = 798.7(1), c = 1926.1(2) pm, β = 107.96(1)°, R1 = 0.0302. 1 contains [Cl3PNPPh3]+ cations with PN bond lengths of 152.5(2) and 160.9(2) pm, and a PNP bond angle of 140.5(1)°. 2 ·CH2Cl2: Space group , Z = 2, lattice dimensions at 193 K: a = 1031.2(1), b = 1448.3(2), c = 1811,4(2) pm, α = 70.96(1)°, β = 87.67(1)°, γ = 75.37(1)°, R1 = 0.0713. 2 ·CH2Cl2 contains cations [SbCl4(HNPPh3)2]+ with octahedrally coordinated Sb atom and the HNPPh3 ligand molecules being in trans‐position. Sb–N bond lengths are 207.6(6) and 209.3(6) pm, PN bond lengths 162.3(7) and 160.8(7), which approximately corresponds with double bonds. 3 ·0.5CH2Cl2: Space group P4/n, Z = 2, lattice dimensions at 193 K: a = b = 1678.8(1), c = 1244.3(1) pm, R1 = 0.0618. 3 ·0.5CH2Cl2 contains [Sb(NPPh3)4]+ cations with tetrahedrally coordinated Sb atom and short Sb–N bond lengths of 193.7(6) pm. The PN distances of the phosphoraneiminato ligands, (NPPh3)? with 156.5(6) pm, correspond with double bonds, the SbNP bond angles are 130.6(3)°. 相似文献
12.
M. S. El‐Shahawi A. S. Bashammakh A. A. Al‐Sibaai S. O. Bahaffi E. H. Al‐Gohani 《Electroanalysis》2011,23(3):747-754
A simple adsorptive cathodic stripping voltammetry method has been developed for antimony (III and V) speciation using 4‐(2‐thiazolylazo) – resorcinol (TAR). The methodology involves controlled preconcentration at pH 5, during which antimony(III) – TAR complex is adsorbed onto a hanging mercury drop electrode followed by measuring the cathodic peak current (Ip,c) at ?0.39 V versus Ag/AgCl electrode. The plot of Ip,c versus antimony(III) concentration was linear in the range 1.35×10?9–9.53×10?8 mol L?1.The LOD and LOQ for Sb(III) were found 4.06×10?10 and 1.35×10?9 mol L?1, respectively. Antimony(V) species after reduction to antimony(III) with Na2SO3 were also determined. Analysis of antimony in environment water samples was applied satisfactorily. 相似文献
13.
Karen A. Ketcham Isabel Garcia Elena Bermejo John K. Swearingen Alfonso Castieiras Douglas X. West 《无机化学与普通化学杂志》2002,628(2):409-415
Reduction of 2‐cyanopyridine by sodium in the presence of 3‐hexamethyleneiminylthiosemicarbazide produces 2‐pyridineformamide 3‐hexamethyleneiminylthiosemicarbazone, HAmhexim. Complexes with nickel(II), copper(II) and palladium(II) have been prepared and the following complexes structurally characterized: [Ni(Amhexim)OAc], [{Cu(Amhexim)}2C4H4O4]·2DMSO·H2O, [Cu(HAmhexim)Cl2] and [Pd(Amhexim)Cl]. Coordination is via the pyridyl nitrogen, imine nitrogen and thiolato or thione sulfur atom when coordinating as the anionic or neutral ligand, respectively. [{Cu(Amhexim)}2C4H4O4] is a binuclear complex with the two copper(II) ions bridged by the succinato group in [Cu‐(HAmhexim)Cl2] the Cu atom is 5‐coordinate and close to a square pyramid structure and in [Ni(Amhexim)OAc] and [Pd(Amhexim)Cl] the metal atoms are planar, 4‐coordinate. 相似文献
14.
Mohammad Yazdanbakhsh Mohammad Hakimi Majid M. Heravi Mitra Ghassemzadeh Bernhard Neumüller 《无机化学与普通化学杂志》2004,630(5):627-629
The reaction of 4‐amino‐1, 2, 4‐triazin‐3(2H)‐thione‐5‐one (ATTO, 1 ) with [Cu(PPh3)2]NO3 in ethanol led to the complex [Cu(PPh3)2(ATTO)]NO3 ( 2 ). 2 was characterized by elemental analyses, IR, 1H NMR and Raman spectroscopy. A single‐crystal X‐ray diffraction of compound 2 revealed that ATTO acts as a bidentate ligand via its nitrogen and sulfur atoms. Crystal data for 2 at 20 °C: space group P21/n with a = 975.7(1), b = 1533.5(2), c = 2504.2(3) pm, β = 92.25(1)°, Z = 4, R1 = 0.0632. 相似文献
15.
Sujittra Youngme Jaturong Phatchimkun Samran Prabpai Chaveng Pakawatchai Palangpon Kongsaeree 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(2):m45-m47
The two new title complexes, [Cu(N3)(dpyam)2]PF6 (dpyam is di‐2‐pyridylamine, C10H11N3), (I), and [Cu(N3)(dpyam)2]Cl·4H2O, (II), respectively, have been characterized by single‐crystal X‐ray diffraction. Both complexes display a distorted square‐pyramidal geometry. Each Cu atom is coordinated in the basal plane by three dpyam N atoms and one azide N atom in equatorial positions, and by another N atom from the dpyam group in the apical position. In complex (I), the one‐dimensional supramolecular architecture is assembled via hydrogen‐bonding interactions between the amine N atom and terminal azide N atoms and the F atoms of the PF6− anion. For complex (II), hydrogen‐bonding interactions between the amine N atom, the Cl− anion and water O atoms result in a two‐dimensional lattice. 相似文献
16.
Gordana Pavlovi Zora Popovi
eljka Soldin Dubravka Matkovi‐alogovi 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(7):801-803
The reaction of 1‐methyl‐1,3‐imidazole‐2‐thione (meimtH) with mercury(II) iodide in methanol in a 2:1 molar ratio resulted in the formation of single crystals of the title compound, [HgI2(C4H6N2S)2]. The Hg atom is coordinated by two I [2.7809 (9) and 2.7999 (8) Å] and two thione S atoms [2.520 (3) and 2.576 (3) Å] with irregular tetrahedral coordination geometry. The NH groups of the imidazole ring take part in intra‐ and intermolecular hydrogen bonds with I atoms [N?I 3.596 (8) and 3.611 (9) Å, respectively] joining molecules into infinite chains parallel to the z axis. 相似文献
17.
Graham Smith 《Acta Crystallographica. Section C, Structural Chemistry》2015,71(2):140-145
The Li, Rb and Cs complexes with the herbicide (2,4‐dichlorophenoxy)acetic acid (2,4‐D), namely poly[[aqua[μ3‐(2,4‐dichlorophenoxy)acetato‐κ3O1:O1:O1′]lithium(I)] dihydrate], {[Li(C8H5Cl2O3)(H2O)]·2H2O}n, (I), poly[μ‐aqua‐bis[μ3‐(2,4‐dichlorophenoxy)acetato‐κ4O1:O1′:O1′,Cl2]dirubidium(I)], [Rb2(C8H5Cl2O3)2(H2O)]n, (II), and poly[μ‐aqua‐bis[μ3‐(2,4‐dichlorophenoxy)acetato‐κ5O1:O1′:O1′,O2,Cl2]dicaesium(I)], [Cs2(C8H5Cl2O3)2(H2O)]n, (III), respectively, have been determined and their two‐dimensional polymeric structures are described. In (I), the slightly distorted tetrahedral LiO4 coordination involves three carboxylate O‐atom donors, of which two are bridging, and a monodentate aqua ligand, together with two water molecules of solvation. Conjoined six‐membered ring systems generate a one‐dimensional coordination polymeric chain which extends along b and interspecies water O—H...O hydrogen‐bonding interactions give the overall two‐dimensional layers which lie parallel to (001). In hemihydrate complex (II), the irregular octahedral RbO5Cl coordination about Rb+ comprises a single bridging water molecule which lies on a twofold rotation axis, a bidentate Ocarboxy,Cl‐chelate interaction and three bridging carboxylate O‐atom bonding interactions from the 2,4‐D ligand. A two‐dimensional coordination polymeric layer structure lying parallel to (100) is formed through a number of conjoined cyclic bridges, including a centrosymmetric four‐membered Rb2O2 ring system with an Rb...Rb separation of 4.3312 (5) Å. The coordinated water molecule forms intralayer aqua–carboxylate O—H...O hydrogen bonds. Complex (III) comprises two crystallographically independent (Z′ = 2) irregular CsO6Cl coordination centres, each comprising two O‐atom donors (carboxylate and phenoxy) and a ring‐substituted Cl‐atom donor from the 2,4‐D ligand species in a tridentate chelate mode, two O‐atom donors from bridging carboxylate groups and one from a bridging water molecule. However, the two 2,4‐D ligands are conformationally very dissimilar, with one phenoxyacetate side chain being synclinal and the other being antiperiplanar. The minimum Cs...Cs separation is 4.4463 (5) Å. Structure extension gives coordination polymeric layers which lie parallel to (001) and are stabilized by intralayer water–carboxylate O—H...O hydrogen bonds. 相似文献
18.
Elena Bermejo Alfonso Castieiras Isabel García‐Santos Douglas X. West 《无机化学与普通化学杂志》2004,630(7):1096-1109
Sodium in dry methanol reduces 2‐cyanopyridine in the presence of 3‐hexamethyleneiminylthiosemicarbazide and produces 2‐pyridineformamide 3‐hexamethyleneiminylthiosemicarbazone, HAmhexim ( 1 ). Complexes with zinc(II ), cadmium(II ) and mercury(II ) have been prepared and characterized by spectroscopic techniques. In addition, the crystal structures of HAmhexim ( 1 ), [Zn(Amhexim)(OAc)]2μ·μDMSO ( 2 ), [Cd(HAmhexim)Cl2]μ·μDMSO ( 7 ), [Cd(Amhexim)2] ( 8 ), [Cd(HAmhexim)Br2]μ·μDMSO ( 9 ), [Cd(HAmhexim)I2]μ·μEtOH ( 10 ), [Hg(HAmhexim)Cl2]μ·μDMSO ( 11 ), [Hg(Amhexim)Br]2 ( 13 ), [Hg3(HAmhexim)(Amhexim)Br5]μ·μH2O ( 14 ) and [Hg(Amhexim)I]2 ( 15 ) have been determined. Coordination of the anionic and neutral thiosemicarbazone ligand occurs through the pyridine nitrogen atom, imine nitrogen atom, and thiolato or thione sulfur atom. In [Zn(Amhexim)(OAc)]2 one of the bridging acetato ligands has monodentate coordination and the other bridges in a bidentate manner. [Cd(Amhexim)2] is a 6‐coordinate species while the other cadmium complexes are 5‐coordinate. In [Hg(Amhexim)Br]2 and [Hg(Amhexim)I]2 the thiolato sulfur atoms act as bridges between the Hg atoms to form dimeric compounds and [Hg3(HAmhexim)(Amhexim)Br5]μ·μH2O is a trinuclear complex with three different centers — two metallic centers have a 5‐coordination and the another one has 4‐coordination. In addition, [Hg(HAmhexim)Cl2]μ·μDMSO and [Hg3(HAmhexim)(Amhexim)Br5]μ·μH2O shown a supramolecular one‐dimensional hydrogen‐bonded self‐assembling. 相似文献
19.
Ibrahim Abdul Razak Anwar Usman Hoong‐Kun Fun Bohari M. Yamin Goh Wooi Keat 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(2):m122-m123
In the title compound, [SbCl2(C4H8N2S)2]Cl, the coordination around the Sb atom can be described as distorted pseudo‐octahedral. Both rings of the trimethylenethiourea ligands [alternatively 3,4,5,6‐tetrahydropyrimidine‐2(1H)‐thione] adopt an envelope conformation. The molecules are connected into dimers in the ab plane by two intermolecular hydrogen bonds. The dimers are arranged into infinite one‐dimensional chains along the a axis as a result of the Cl? ions forming intermolecular hydrogen bonds with three NH groups. 相似文献
20.
Gordana Pavlovi Zora Popovi
eljka Soldin Dubravka Matkovi‐alogovi 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(1):61-63
The Hg atom in the title monomeric complex, dichlorobis(3‐imidazolium‐2‐thiolato‐S)mercury(II), [HgCl2(C3H4N2S)2], is four‐coordinate having an irregular tetrahedral geometry composed of two Cl atoms [Hg—Cl 2.622 (2) and 2.663 (2) Å] and two thione S atoms [Hg—S 2.445 (2) and 2.462 (2) Å]. The monodentate thione ligand adopts a zwitterionic form and exists as the 3‐imidazolium‐2‐thiolate ion. The bond angle S1—Hg—S2 of 130.87 (8)° has the greatest deviation from ideal tetrahedral geometry. Intermolecular hydrogen bonds between two of the four N—H groups and one of the Cl atoms [3.232 (8) and 3.238 (7) Å] stabilize the crystal structure, while the other two N—H groups contribute through the formation of N—H?Cl intramolecular hydrogen bonds with the other Cl atom [3.121 (7) and 3.188 (7) Å]. 相似文献