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1.
The coordination chemistry of beryllium with particular emphasis on chelates under physiological or near physiological conditions is surveyed. Hard donors such as oxygen are emphasized; equilibrium data and formation constants are reported as an indication of the strength of the complex. 相似文献
2.
J. D. Woollins 《Polyhedron》1984,3(12):1365-1367
Deprotonation of heptasulphurmonoimide at −78°C using BuLi followed by reaction with HAuCl4 yields AuCl2(S3N), in moderate yield (21%), characterised by IR/Raman and UV/Vis spectroscopies. 相似文献
3.
J. Novosad J. Jandl J. D. Woollins 《Journal of Radioanalytical and Nuclear Chemistry》1992,165(5):287-294
Samples of clinoptilolite were modified using insoluble hexacyanoferrate from aqueous solution. The modified samples were characterized by elemental analysis, powder X-ray diffraction, solid state NMR and vibrational spectroscopy. The sorption properties of modified clinoptilolite were studied, too. Higher affinity for137Cs sorption in comparison with the natural clinoptilolite has been proved. 相似文献
4.
5.
Reaction of Hg(S7N)2 with cis- PtCl2(PR3)2 (PR3 = PPh3, PPh2Me, PPHMe2, PEt3) in the presence of Na[PF6] gives [Pt(S3N)(PR3)2][PF6] in 32–46% yield. The complexes have been characterized by IR, NMR and microanalyses. The X-ray crystal structures of two examples (PR3 = PPh2Me and PEt3) show that the S3N− ligand coordinates in a bidentate fashion via two sulphur atoms. 相似文献
6.
Jain SL Bhattacharyya P Milton HL Slawin AM Crayston JA Woollins JD 《Dalton transactions (Cambridge, England : 2003)》2004,(6):862-871
Seven new pyridine dicarboxamide ligands H2L(1-7) have been synthesised from condensation reactions involving pyridine-2,6-dicarboxylic acid (H2dipic), pyridine-2,6-dicarbonyl dichloride or 2,6-diaminopyridine with heterocyclic amine or carboxylic acid precursors. Crystallographic analyses of N,N'-bis(2-pyridyl)pyridine-2,6-dicarboxamide monohydrate (H2L8 x H2O), N,N'-bis[2-(2-pyridyl)methyl]pyridine-2,6-dicarboxamide and N,N'-bis[2-(2-pyridyl)ethyl]pyridine-2,6-dicarboxamide monohydrate revealed extensive intramolecular hydrogen bonding interactions. 2,6-Bis(pyrazine-2-carboxamido)pyridine (H2L6) and 2,6-bis(pyridine-2-carboxamido)pyridine (H2L7) reacted with copper(II) acetate monohydrate to give tricopper(II) complexes [Cu3(L)2(mu2-OAc)2]. X-Ray crystallography confirmed deprotonation of the amidic nitrogen atoms and that the (L6,7)2- ligands and acetate anions hold three copper(II) ions in approximately linear fashion. H2L8. Reacted with copper(II) tetrakis(pyridine) perchlorate to give [Cu(L8)(OH2)]2 x 2H2O, in which (L8)2- was tridentate through the nitrogen atoms of the central pyridine ring and the deprotonated carboxamide groups at one copper centre, with one of the terminal pyridyl rings coordinating to the other copper atom in the dimer. The corresponding reaction using H2L7 gave [Cu3(L7)2(py)2][ClO4]2, which transformed during an attempted recrystallisation from ethanol under aerobic conditions to a tetracopper(II) complex [Cu4(L7)2(L7-O)2]. 相似文献
7.
The ligands [Ph2P(O)NP(E)Ph2]− (E=S I; E=Se II) can readily be complexed to a range of palladium(II) starting materials affording new six-membered Pd–O–P–N–P–E palladacycles. Hence ligand substitution reaction of the chloride complexes [PdCl2(bipy)] (bipy=2,2′-bipyridine), [{Pd(μ-Cl)(L–L)}2] (HL–L=C9H13N or C12H13N), [{Pd(μ-Cl)Cl(PMe2Ph)}2] or [PdCl2(PR3)2] [PR3=PPh3; 2PR3=Ph2PCH2CH2PPh2or cis-Ph2PCH=CHPPh2] with either I (or II) in thf or CH3OH gave [Pd{Ph2P(O)NP(E)Ph2-O,E}(bipy)]PF6, [Pd{Ph2P(O)NP(E)Ph2-O,E}(L–L)], [Pd{Ph2P(O)NP(E)Ph2-O,E}Cl(PMe2Ph)] or [Pd{Ph2P(O)NP(E)Ph2-O,E} (PR3)2]PF6 in good yields. All compounds described have been characterised by a combination of multinuclear NMR [31 P{1 H} and 1 H] and IR spectroscopy and microanalysis. The molecular structures of five complexes containing the selenium ligand II have been determined by single-crystal X-ray crystallography. Three different ring conformations were observed, a pseudo-butterfly, hinge and in the case of all three PR3 complexes, pseudo-boat conformations. Within the Pd–O–P–N–P–Se rings there is evidence for π-electron delocalisation. 相似文献
8.
Aragoni MC Arca M Devillanova FA Isaia F Lippolis V Mancini A Pala L Slawin AM Woollins JD 《Inorganic chemistry》2005,44(26):9610-9612
We report the first examples of metal dithiolenes belonging to the class [M(R-dmet)(2)] [R-dmet = formally monoreduced N-substituted thiazolidine-2,4,5-trithione; R = Et, M = Ni (1), Pd (2), Pt (3)]. A comparative spectroscopic, electrochemical, and density functional theory theoretical investigation indicates that [M(R-dmet)(2)] complexes show features intermediate between those of the dithiolenes belonging to the previously reported classes [M(R,R'-timdt)(2)] and [M(dmit)(2)] (R,R'-timdt = formally monoreduced N,N'-disubstituted imidazolidine-2,4,5-trithione; dmit = 2-thioxo-1,3-dithiole-4,5-dithiolato). UV-vis-near-IR spectroscopy and cyclic voltammetry/differential pulsed voltammetry measurements performed on 1 and 3 proved that the new dithiolenes are stable as neutral, monoanionic, and bianionic species and feature a near-IR electrochromic absorption falling at about 1000 and 1250 nm for neutral and monoanionic species, respectively. 相似文献
9.
Aucott SM Kilian P Milton HL Robertson SD Slawin AM Woollins JD 《Inorganic chemistry》2005,44(8):2710-2718
Titanocene 1,8-dithiolato-naphthalene and titanocene 2,2'-dithiolato biphenyl are produced by the reaction of naphtho[1,8-cd]-1,2-dithiole [or the biphenyl] with titanocene dicarbonyl (Ti(II)) in toluene at room temperature. The pro-ligands 2,7-di(tert-butyl)naphtho[1,8-cd]-1,2-dithiole, 5,6-dihydroacenaphtho[5,6-cd]-1,2-dithiole, 4,5-dithioacephenanthrylene, and 13,14-dithiapicene have been used in similar reactions with titanocene dicarbonyl to investigate the effect of steric bulk and of varying the naphthalene backbone on the final complex. The resulting Cp(2)TiS(2)Ar complexes (Ar = naphthalene) have been shown by temperature-dependent (1)H NMR spectroscopy to exist in solution in an envelope conformation with the six-membered TiS(2)C(3) rings undergoing inversion on the NMR time scale while the similar Cp(2)TiS(2)Ar complexes (Ar = biphenyl, binaphthalene) interconvert more rapidly. Titanocene 2,2'-disulfinato biphenyl has been synthesized by the salt elimination reaction of titanocene dichloride (Ti(IV)) and the disodium salt of biphenyl 2,2'-disulfinic acid. Finally, the effect of using pro-ligands where the sulfur atoms have been mono- or di-oxidized has been studied, and an interesting oxygen elimination reaction is observed for the S=O fragments but not for the SO(2) groups. All complexes have been characterized spectroscopically and seven X-ray structures are reported. 相似文献
10.