共查询到20条相似文献,搜索用时 31 毫秒
1.
Christoph E. Strasser 《Journal of organometallic chemistry》2006,691(22):4788-4796
The first gold(I) trithiophosphite complexes were synthesised and fully characterised. Reaction of (tht)AuX (X = Cl, C6F5; tht = tetrahydrothiophene) with trithiophosphites (RS)3P (R = Me, Ph) and the bicyclic [(SCH2CH2S)PSCH2]2 (2L) afforded the corresponding molecular complexes (RS)3PAuX [R = Me, X = Cl (1); R = Me, X = C6F5 (2); R = Ph, X = Cl (3); R = Ph, X = C6F5 (4)], and 2L(AuX)2 [X = Cl (5), X = C6F5 (6)]. Reacting (tht)AuCl consecutively with two mole equivalents of (MeS)3P and then AgOTf, gave the ionic compound {[(MeS)3P]2Au}OTf (7). The compounds were characterised by multinuclear NMR spectroscopy, IR measurements and mass spectrometry, and the crystal and molecular structures of 1, 3, 6, two polymorphs of 2 as well as the known (MeO)3PAuCl (8) were determined by X-ray diffraction. The halide complexes 1 and 8 are isostructural and exhibit infinite chains of “crossed-sword”-type aurophilic interactions with Au?Au contact distances of 3.2942(3) and 3.1635(4) Å, respectively. Complex 6 exhibits a long Au?Au contact of 3.4671(9) Å. Au?S interactions between 3.3455(7) and 3.520(2) Å are present in the structures of 1 and one polymorph of 2. 相似文献
2.
Ya Chen Jian-Shi Jin Zhi-Gang Zou Xiao-Zeng You 《Journal of organometallic chemistry》2009,694(5):763-43
Rhenium(I) tricarbonyl complexes with bispyridine ligands bearing sulfur-rich pendant, Re(CO)3(Medpydt)X (Medpydt = dimethyl 2-(di(2-pyridyl)methylene)-1,3-dithiole-4,5-dicarboxylate; X = Cl, 1; X = Br, 2) and Re(CO)3(MebpyTTF)X (MebpyTTF = 4,5-bis(methyloxycabonyl)-4′,5′-(4′-methyl-2,2′-dipyrid-4-ylethylenedithio)-tetrathiafulvalene; X = Cl, 5; X = Br, 6), were prepared from the reactions between Re(CO)5X (X = Cl, Br) and Medpydt or MebpyTTF, respectively. Hydrolysis of the above complexes afforded the analogues with carboxylate derivatives, Re(CO)3(H2dpydt)X (X = Cl, 3; X = Br, 4) and Re(CO)3(H2bpyTTF)X (X = Cl, 7; X = Br, 8). The crystal structures for complexes 1 · 2H2O, 5 and 6 were determined using X-ray single crystal diffraction. UV-Vis absorption spectra of the rhenium complexes show the intraligand and MLCT transitions. Electrochemical behaviors of all new compounds were studied with cyclic voltammetry. Upon irradiation, complexes 3-6 exhibit blue to red emissions in fluid solutions at the room temperature. The performance of complexes 3, 4, 7 and 8 as photosensitizers for anatase TiO2 solar cells was preliminarily investigated as well. 相似文献
3.
Copper(I) complexes of short-bite aminobis(phosphonite), PhN{P(–OC10H6(μ-S)C10H6O–)}2 (1) have been synthesized. Reactions of 1 with an excess of CuX (X = Cl, Br, and I) afforded the ligand-bridged binuclear complexes, [PhN(PR-κP)2{Cu(μ-X)(MeCN)}2] (2, X = Cl; 3, X = Br; 4, X = I; R = –OC10H6(μ-S)C10H6O–), whereas treatment with 0.5 equiv. of [Cu(MeCN)4]PF6 produces the mononuclear bischelated cationic complex, [{PhN(PR-κP)2}2Cu](PF6) (5). Single crystal X-ray structures of complexes 3 and 4 are reported. Complex 3 shows strong π–π stacking interactions between the naphthyl moieties, whereas complex 4 shows ligand-supported Cu?Cu metallophilic interactions. 相似文献
4.
Wen-Qian Geng Hong-Ping Zhou Long-Huai ChengFu-Ying Hao Guo-Yi XuFei-Xia Zhou Zhi-Peng YuZheng Zheng Jian-Qing WangJie-Ying Wu Yu-Peng Tian 《Polyhedron》2012,31(1):738-747
Six novel organotin(IV) carboxylates have been successfully synthesized, namely, the polymer (C6H5)3Sn(L1)∞ (1) [HL1 = 4-imidazolyl benzoic acid], the mononuclear (C6H5)3Sn(L2) (2) [HL2 = 4-pyrazolylbenzoic acid], (C6H5)3Sn(L3)·CH3OH (3) [HL3 = 4-triazolylbenzoic acid] and (C6H5)3Sn(L4) (4) [HL4 = 4-tetrazolyl benzoic acid] and the tetranuclear [(n-Bu2Sn)4(L2)2O2(OCH3)2] (5) and [(n-Bu2Sn)4(L3)2O2(OCH3)2] (6). X-ray diffraction analyses show 1D infinite chain of polymer 1, single molecular structures of isomorphous complexes 2 and 4, single molecule structures of complex 3 containing solvent CH3OH molecule and similar ladder-type structures of complexes 5 and 6. The photoluminescence of ligands and 1-6 were also measured in the solid state at room temperature. 相似文献
5.
Ashok K.S. Chauhan Anamika Ramesh C. Srivastava Jens Beckmann Andrew Duthie 《Journal of organometallic chemistry》2005,690(5):1350-1355
The unsymmetrically substituted diorganotellurium dihalides [2-(4,4′-NO2C6H4CHNC6H3Me]RTeX2 (R = 4-MeOC6H4, X = Cl, 1a; Br, 1b; I, 1c; R = 4-MeC6H4; X = Cl, 2; R = C6H5, X = Cl, 3) were prepared in good yields and characterized by solution and solid-state 125Te NMR spectroscopy, IR spectroscopy and X-ray crystallography. In the solid-state, molecular structures of 1a and 1c possess scarcely observed 1,4-type intramolecular Te?N secondary interaction. Crystal packing of these compounds show an unusually rich diversity of intermolecular secondary, Te?O, Te?I and I?I interactions, Te?π contacts as well as extensive π-stacking of the organic substituents. 相似文献
6.
Ryo Horikoshi 《Journal of organometallic chemistry》2005,690(7):1793-1799
5-Ferrocenylpyrimidine (FcPM) reacts with dinuclear copper(II) carboxylates ([Cu2(RCOO)4]; R = C6H5, C5H11, CH3) to produce one-dimensional coordination polymers [Cu2(C6H5COO)4(FcPM)]n (1), [Cu2(C5H11COO)4(FcPM)]n · nCH3CN (2), and a discrete tetranuclear complex [Cu2(CH3COO)4(FcPM)2] (3). Compounds 1 and 2 show similar zigzag chain structures, comprising alternate linking of FcPM and dinuclear copper(II) units, whereas the structure of 3 corresponds to the local structural motifs of 1 and 2. Reaction of FcPM with zinc salts (ZnX2; X = NO3, SCN) affords zinc-centered ferrocenyl cluster complexes, [Zn(NO3)2(FcPM)3] (4) and [Zn(SCN)2(FcPM)2] · 0.5H2O (5), with varying M:L ratios. FcPM acts as a bidentate ligand in 1 and 2, and as a monodentate ligand in the others. 相似文献
7.
Fu-Chen Liu Tu-Chieh Tsai Chen-Shiang Lee Ju-Chun Wang 《Journal of organometallic chemistry》2010,695(3):423-4290
Mononuclear compounds M(CO)2(η3-C3H5)(en)(X) (X = Br, M = Mo(1), W(2); X = N3, M = Mo(3), W(4); X = CN, M = Mo(5), W(6)) and cyanide-bridged bimetallic compounds [(en)(η3-C3H5)(CO)2M(μ-CN)M(CO)2(η3-C3H5)(en)]Br (M = Mo (7), W(8)) were prepared and characterized. These compounds are fluxional and display broad unresolved proton NMR signals at room temperature. Compounds 1-6 were characterized by NMR spectroscopy at −60 °C, which revealed isomers in solution. The major isomers of 1-4 adopt an asymmetric endo-conformation, while those of 5 and 6 were both found to possess a symmetric endo-conformation. The single crystal X-ray structures of 1-6 are consistent with the structures of the major isomer in solution at low temperature. In contrast to mononuclear terminal cyanide compounds 5 and 6, cyanide-bridged compounds 7 and 8 were found to adopt the asymmetric endo-conformation in the solid state. 相似文献
8.
Jérôme Canivet 《Journal of organometallic chemistry》2005,690(13):3202-3211
The monocationic chloro complexes containing chelating 1,10-phenanthroline (phen) ligands [(arene)Ru(N∩N)Cl]+ (1: arene = C6H6, N∩N = phen; 2: arene = C6H6, N∩N = 5-NO2-phen; 3: arene = p-MeC6H4Pri, N∩N = phen; 4: arene = p-MeC6H4Pri, N∩N = 5-NO2-phen; 5: arene = C6Me6, N∩N = phen; 6: arene = C6Me6, N∩N = 5-NO2-phen; 7: arene = C6Me6, N∩N = 5-NH2-phen) have been prepared and characterised as the chloride salts. Hydrolysis of these chloro complexes in aqueous solution gave, upon precipitation of silver chloride, the corresponding dicationic aqua complexes [(arene)Ru(N∩N)(OH2)]2+ (8: arene = C6H6, N∩N = phen; 9: arene = C6H6, N∩N = 5-NO2-phen; 10: arene = p-MeC6H4Pri, N∩N = phen; 11: arene = p-MeC6H4Pri, N∩N = 5-NO2-phen; 12: arene = C6Me6, N∩N = phen; 13: arene = C6Me6, N∩N = 5-NO2-phen; 14: arene = C6Me6, N∩N = 5-NH2-phen), which have been isolated and characterised as the tetrafluoroborate salts. The catalytic potential of the aqua complexes 8-14 for transfer hydrogenation reactions in aqueous solution has been studied: complexes 12 and 14 catalyse the reaction of acetophenone with formic acid to give phenylethanol and carbon dioxide with turnover numbers around 200 (80 °C, 7 h). In the case of 12, it was possible to observe the postulated hydrido complex [(C6Me6)Ru(phen)H]+ (15) in the reaction with sodium borohydride; 15 has been characterised as the tetrafluoroborate salt, the isolated product [15]BF4, however, being impure. The molecular structures of [(C6Me6)Ru(phen)Cl]+ (1) and [(C6Me6)Ru(phen)(OH2)]2+ (12) have been determined by single-crystal X-ray structure analysis of [1]Cl and [12](BF4)2. 相似文献
9.
Ni(II) complexes (1–5) of di-2-pyridyl ketone N(4)-phenylthiosemicarbazone (HL) have been synthesized and spectrochemically characterized. Elemental analyses revealed a NiL2 · 2H2O stoichiometry for compound 1. However, the single crystals isolated revealed a composition NiL2 · 0.5(H2O)0.5(DMF). The compound crystallizes into a monoclinic lattice with the space group P21/n. Complexes 2, 3 and 4 are observed to show a 1:1:1 ratio of metal:thiosemicarbazone:gegenion, with the general formula NiLX · yH2O [X = NCS, y = 2 for 2; X = Cl, y = 3 for 3 and X = N3, y = 4.5 for 4]. Compound 5 is a dimer with a metal:thiosemicarbazone:gegenion ratio of 2:2:1, with the formula [Ni2L2(SO4)] · 4H2O. 相似文献
10.
A kinetic study of the reaction of hydroxide ion with (CO)5MoC(XCH2CH2OH)(C6H5) (X = O for Mo-OR, and X = S for Mo-SR), and (CO)5WC(OCH2CH2OH)(C6H4-Z) (W-OR(Z)) is reported. The results are consistent with a pathway in basic solution that involves rapid deprotonation of the OH group followed by rate-limiting cyclization. The parameter k1KOH for the reaction of W-OR(Z) was determined as a function of the phenyl substituents. They were found to correlate well with the Hammett equation. The dependence of the reactivity on the metal atoms in the complexes M-OR (M = Cr, Mo and W) shows that the reactivity decreases slightly down the group of the Periodic Table, while for M-SR the reactivity increases slightly down the group. A plausible explanation of these results is offered based on electronegativity values of the metal atoms. The much higher ρ(k1KOH) value for W-OR(Z) over W-SR(Z) arises mainly due to the stabilization of the reactant carbene complex by the stronger π-donor effect of oxygen over sulfur. 相似文献
11.
A series of silver coordination polymers constructed from flexible bis(benzimidazole) ligands and different carboxylates 总被引:1,自引:0,他引:1
In this article, eight new silver coordination polymers constructed from two structurally related ligands, 1,1′-(1,4-butanediyl)bis(2-methylbenzimidazole) (bbmb) and 1,1′-(1,4-butanediyl)bis(2-ethylbenzimedazole) (bbeb), have been synthesized: [Ag(L1)(bbmb)]·C2H5OH·H2O (1), [Ag(L2)(bbmb)]·C2H5OH (2), [Ag(L3)(bbmb)] (3), [Ag2(L4)(bbmb)2]·C2H5OH (4), [Ag(L2)(bbeb)]·C2H5OH (5), [Ag(L5)(bbeb)]·CH3OH (6), [Ag2(L6)2(bbeb)]·H2O (7), and [Ag2(L7)(bbeb)2]·4(H2O) (8), where L1 = benzoate anion, L2 = p-methoxybenzoate anion, L3 = 2-amino-benzoate anion, L4 = oxalate anion, L5 = cinnamate ainon, L6 = 3-amino-benzoate anion, and L7 = fumaric anion. In 1-3, 5 and 6, the bidentate N-donor ligands (bbmb and bbeb) in trans conformations bridge neighboring silver centers to form 1D single chain structures. The carboxylate anions are attached on both sides of the chains. Moreover, 1 and 3 are extended into 2D layers, while 2 and 6 are extended into 3D frameworks through π-π interactions. In 4, the bbmb ligands bridge adjacent Ag(I) centers to form -Ag-bbmb-Ag- chains, which are further connected by L4 anions to form a 2D layer. The resulting layers are extended into 3D frameworks through strong π-π interactions. In 7, the N-donor ligands (bbeb) in trans conformations bridge two silver centers to generate a [Ag2(bbeb)]2+ unit. The adjacent [Ag2(bbeb)]2+ units are further connected via the L6 anions to form a 1D ladder chain. Moreover, the structure of compound 7 is extended into a 3D framework through hydrogen bonding and π-π interactions. In 8, two Ag(I) cations are bridged by two bbeb ligands in cis conformations to form a [Ag2(bbeb)2]2+ ring, which are further linked by L7 anions to generate a 1D string chain. Furthermore, the hydrogen bonding and π-π interactions link L7 anions to form a 2D supramolecular sheet. Additionally, the luminescent properties of these compounds were also studied. 相似文献
12.
Ara Núñez-MontenegroRosa Carballo José M. Hermida-RamónEzequiel M. Vázquez-López 《Polyhedron》2011,30(12):2146-2156
N-thioamide thiosemicarbazone derived from 4-(methylthio)benzaldehyde (R = H, HL1; R = Me, HL2 and R = Ph, HL3) have been prepared and their reaction with fac-[ReX(CO)3(CH3CN)2] (X = Br, Cl) in methanol gave the adducts [ReX(CO)3(HLn)] (1a X = Cl, n = 1; 1a′ X = Br, n = 1; 1b X = Cl, n = 2; 1b′ X = Br, n = 2; 1c X = Cl, n = 3; 1c′ X = Br, n = 3) in good yield.All the compounds have been characterized by elemental analysis, mass spectrometry (ESI), IR and 1H NMR spectroscopic methods. Moreover, the structures of HL2, HL3, HL3·(CH3)2SO and 1b′·H2O were also elucidated by X-ray diffraction. In 1b′, the rhenium atom is coordinated by the sulphur and the azomethine nitrogen atoms (κS,N3) forming a five-membered chelate ring, as well as three carbonyl and bromide ligands. The resulting coordination polyhedron can be described as a distorted octahedron.The structure of the dimers is based on rhenium(I) thiosemicarbazonates [Re2(L1)2(CO)6] (2a), [Re2(L2)2(CO)6] (2b) and [Re2(L3)2(CO)6] (2c) as determined by X-ray studies. Methods of synthesis were optimized to obtain amounts of these thiosemicarbazonate complexes. In these compounds the dimer structures are achieved by Re-S-Re bridges, where S is the thiolate sulphur from a κS,N3-bidentate thiosemicarbazonate ligand.Some single crystals isolated in the synthesis of 2b contain [Re(L4)(L2)(CO)3] (3b) where L4 (=2-methylamine-5-(para-methylsulfanephenyl)-1,3,4-thiadiazole) is originated in a cyclization process of the thiosemicarbazone. Furthermore, the rhenium atom is coordinate by the sulphur and the thioamidic nitrogen of the thiosemicarbazonate (κS,N2) affording a four-membered chelate ring. 相似文献
13.
Reaction of the benzene-linked bis(pyrazolyl)methane ligands, 1,4-bis{bis(pyrazolyl)-methyl}benzene (L1) and 1,4-bis{bis(3-methylpyrazolyl)methyl}benzene (L2), with pentamethylcyclopentadienyl rhodium and iridium complexes [(η5-C5Me5)M(μ-Cl)Cl]2 (M = Rh and Ir) in the presence of NH4PF6 results under stoichiometric control in both, mono and dinuclear complexes, [(η5-C5Me5)RhCl(L)]+ {L = L1 (1); L2 (2)}, [(η5-C5Me5)IrCl(L)]+ {L = L1 (3); L2 (4)} and [{(η5-C5Me5)RhCl}2(μ-L)]2+ {L = L1 (5); L2 (6)}, [{(η5-C5Me5)IrCl}2(μ-L)]2+ {L = L1 (7); L2 (8)}. In contrast, reaction of arene ruthenium complexes [(η6arene)Ru(μ-Cl)Cl]2 (arene = C6H6, p-iPrC6H4Me and C6Me6) with the same ligands (L1 or L2) gives only the dinuclear complexes [{(η6-C6H6)RuCl}2(μ-L)]2+ {L = L1 (9); L2 (10)}, [{(η6-p-iPrC6H4Me)RuCl}2(μ-L)]2+ {L = L1 (11); L2 (12)} and [{(η6-C6Me6)RuCl}2(μ-L)]2+ {L = L1 (13); L2 (14)}. All complexes were isolated as their hexafluorophosphate salts. The single-crystal X-ray crystal structure analyses of [7](PF6)2, [9](PF6)2 and [11](PF6)2 reveal a typical piano-stool geometry around the metal centers with six-membered metallo-cycle in which the 1,4-bis{bis(pyrazolyl)-methyl}benzene acts as a bis-bidentate chelating ligand. 相似文献
14.
Jérémie D.A. Pelletier 《Journal of organometallic chemistry》2008,693(16):2723-2731
Both symmetrical and unsymmetrical tetramethylphenyl-linked iminopyridines, 1,4-{(2-C5H4N)RCN}2-2,3,5,6-Me4C6 [R = H (L1a), Me (L1b)] and 1-{(2-C5H4N)HCN}-4-{(2-C5H4N)MeCN}-2,3,5,6-Me4C6 (L1c), have been prepared in good yield using straightforward condensation strategies. The molecular structures of L1a and L1c reveal the adjacent imino and pyridyl nitrogen atoms to adopt transoid configurations. Interaction of L1x with two equivalents of NiX2 [NiX2 = (DME)NiBr2 (DME = 1,2-dimethoxyethane), NiCl2] in n-BuOH at elevated temperature affords the paramagnetic bimetallic complexes, [(L1x)Ni2X4] [L1x = L1a, X = Br (1a); L1x = L1b, X = Br (1b); L1x = L1c, X = Br (1c); L1x = L1a, X = Cl (1d)] in moderate to good yield. Adduct formation results on treatment of bromide-containing 1a-1c with DMF (dimethylformamide) to yield dicationic [(L1x)Ni2Br2(DMF)6]Br2 [L1x = L1a (2a), L1b (2b), L1c (2c)], while with chloride-containing 1d the neutral species [(L1a)Ni2Cl4(DMF)4] (3) is obtained. Activation of 1a-1d and 2c with excess methylaluminoxane (MAO) generates active ethylene polymerisation catalysts (1b/MAO > 1c/MAO > 1a/MAO ∼ 1d/MAO > 2c/MAO) affording mixtures of waxes and low molecular weight solid polyethylene. Multinuclear NMR and GC analysis of the waxy components reveal methyl branched materials that contain mostly internal unsaturation along with low levels of α-olefins. Broad molecular weight distributions are observed for all the polymers obtained, with that from 1b/MAO leading to the highest molecular weight. Single crystal X-ray diffraction studies have been performed on L1a, L1c, 2a-2c and 3. 相似文献
15.
16.
The ortho-metallated complexes [Pd2{κ2(C,C)-C6H4(PPh2CHC(O)C6H5R}2(μ-Cl)2] (R = Ph (1a), NO2 (1b), Br (1c)) were prepared by refluxing equimolar mixtures of Ph3PCHC(O)C6H5R, (R = Ph, NO2, Br) and Pd(OAc)2 in MeOH, followed by an excess of NaCl. The dinuclear complexes (1a-1c) react with silver trifluoromethylsulfonate and bidentate ligands [L = bipy (2,2′-bipyridine), phen (phenanthroline), dppe (bis(diphenylphosphino)ethane), dppp (bis(diphenylphosphino)propane)] giving the mononuclear stabilized orthopalladated complexes in endo position [Pd{κ2(C,C)-C6H4(PPh2CHC(O)R}L](OTf) [R = Ph, L = phen (2a), bipy (3a), dppe (4a), dppp (5a); R = NO2, L = phen (2b), bipy (3b), dppe (4b), dppp (5b); R = Br, L = phen (2c), bipy (3c), dppe (4c), dppp (5c); OTf = trifluoromethylsulfonate anion]. Orthometalation and ylidic C-coordination are demonstrated by an X-ray diffraction study of 2c and 3c. In the structures, the palladium atom shows a slightly distorted square-planar coordination geometry. 相似文献
17.
Katerina N. Lazarou Iordanis Chadjistamatis Aris Terzis Spyros P. Perlepes Catherine P. Raptopoulou 《Polyhedron》2010
The use of succinamic acid (H2sucm)/N,N′-chelate (2,2′-bipyridine, bpy; 4,4′-dimethyl-2,2′-bipyridine, dmbpy; 1,10-phenanthroline, phen) ‘ligand blends’ in CuX2·yH2O (X = NO3, y = 3; X = Cl, y = 0) chemistry has yielded the new complexes [Cu2(Hsucm)3(bpy)2](NO3)·0.5MeOH (1·0.5MeOH), [Cu2(Hsucm)(OH)Cl(bpy)2](OH)·3.6H2O (5·3.6H2O) and [Cu2(Hsucm)2Cl2(phen)2] (6). The succinamate(−1) ion behaves as a carboxylate ligand and exists in two different coordination modes in the structures of the above complexes, i.e., the common syn, syn μ2-κO:κO′ in 1, 5 and 6, and the μ2-κ2O:κO′ in 1. The primary amide group of Hsucm− remains uncoordinated and participates in intermolecular hydrogen bonding interactions leading to 1D, 2D and 3D networks. Characteristic IR bands of the complexes are discussed in terms of the known structures and the coordination modes of the Hsucm− ligands. 相似文献
18.
Avelina Arnanz Consuelo Moreno Allan J. Lough Salomé Delgado 《Journal of organometallic chemistry》2004,689(20):3218-3231
The reaction between 2,5-bis(trimethylsilylethynyl)thiophene and Co2(CO)8 or Co2(CO)6(X), (X = dppa, dppm), gave rise to the formation of substituted ethynylcobalt complexes containing one or two Co2(CO)6 or Co2(CO)4(X) units, 2-[Co2(CO)4(X){μ2-η2-(SiMe3)C2}]-5-(Me3SiCC)C4H2S (X = 2CO (1), dppa (3) or dppm (4)) and 2,5-[Co2(CO)4(X){μ2-η2-SiMe3C2}]2C4H2S (X = 2CO (2), dppa (5) or dppm (6)). Desilylation of the non-metallated and metallated alkynes in 3, 4 and 6 occurred on treatment with KOH and tetrabutylammonium fluoride to give 2-[Co2(CO)4(μ-X){μ2-η2-SiMe3C2}]-5-(CCH)C4H2S (X = dppa (7), dppm (8)) and 2,5-[Co2(CO)4(μ-dppm){μ2-η2-HC2}]2C4H2S (9), respectively. Crystals of 6 suitable for single-crystal X-ray diffraction were grown and the molecular structure of this compound is discussed. A comparative electrochemical study of all these complexes is presented by means of the cyclic and square-wave voltammetry techniques. 相似文献
19.
Clovis Peppe Fabiano Molinos de Andrade Jaqueline Pinto Vargas Melina de Azevedo Mello Railander Alves Barcellos Robert A. Burrow Rubia Mara Siqueira da Silva 《Journal of organometallic chemistry》2009,694(14):2228-2233
Halogenomethyl-dihalogen-indium(III) compounds X2InCH2X (X = Br, I) obtained from indium monohalides and methylene dihalides were reacted with the soft donor ligands dialkylsulfides, R2S (R = CH3, CH2Ph) to afford the corresponding dialkylsulfonium methylide complexes of InX3, X3InCH2SR2 (X = Br, R = CH3, 1; X = I, R = CH3, 2; X= I, R = CH2Ph, 3). Compound 1 was reacted with the hard donor ligands dimethylsulfoxide or triphenylphosphine oxide to give the corresponding 1:1 adduct, Br3(L)InCH2S(CH3)2 (L = (CH3)2SO, 4; L = (C6H5)3PO, 5). Compounds 1-5 were fully characterized in solution by NMR spectroscopy and in the solid state by X-ray methods. 相似文献
20.
Anshu Singhal Dimple P. Dutta Shaikh M. Mobin Ingo Lieberwirth 《Journal of organometallic chemistry》2007,692(23):5285-5294
In an effort to find simple and common single-source precursors for palladium sulfide nanostructures, palladium(II) complexes, [Pd(S2X)2] (X = COMe (1), COiPr (2)) and η3-allylpalladium complexes with xanthate ligands, [(η3-CH2C(CH3)CR2)Pd(S2X)] (R = H, X = COMe (3); R = H, X = COEt (4); R = H, X = COiPr (5); R = CH3, X = COMe (6)), have been investigated. The crystal structures of [Pd(S2X)2] (X = COMe (1), CoiPr (2)) and [(η3-CH2C(CH3)CH2)Pd(S2COMe)] (3) have been established by single crystal X-ray diffraction analysis. The complexes, 1, 2 and 3 all contain a square planar palladium(II) centre. In the allyl complex 3, this is defined by the two sulfurs of the xanthate and the outer carbons of the 2-methylallyl ligand, while in the complexes, 1 and 2 it is defined by the four sulfur atoms of the xanthate ligand. Thermogravimetric studies have been carried out to evaluate the thermal stability of η3-allylpalladium(II) analogues. The complexes are useful precursors for the growth of nanocrystals of PdS either by furnace decomposition or solvothermolysis in dioctyl ether. The solvothermal decomposition of complexes in dioctyl ether gives a new metastable phase of PdS which can be transformed to the more stable tetragonal phase at 320 °C. The nanocrystals obtained have been characterized by PXRD, SEM, TEM and EDX. 相似文献