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61.
Anne Astier Jean-Claude Daran Yves Jeannin Catherine Rigault 《Journal of organometallic chemistry》1983,241(1):53-68
Syntheses and single-crystal X-ray diffraction studies have been completed on two cycloruthenapentadienyl (CO)6Ru2L2 derivatives, with L = CH2OHC = CCH2OH and C2H5C=CCH2CH2OH respectively. Crystal data are as follows: for [(CO)3RuC4(CH2OH)4]Ru(CO)3·H2O, P21/c, a 13.72(1), b 9.501(4), c 14.86(1) Å, β 101.10(6)°, Rw = 0.052 for 1911 reflections; for [(CO)3RuC4(CH2CH2OH)2(C2H5)2]Ru(CO)3, P21/c, a 9.191(3), b 16.732(4), c 14.903(3) Å, β 113.61(4)°, Rw = 0.042 for 2865 reflections. Both compounds are built up from binuclear units, each unit being regarded as a Ru(CO)3 fragment π-bonded to a cycloruthenapentadienyl ring. The molecular parameters are compared with those of known cyclometallapentadienyl complexes of transition metals. The presence of a semi-bridging CO group is discussed. 相似文献
62.
63.
Canac Y Conejero S Donnadieu B Schoeller WW Bertrand G 《Journal of the American Chemical Society》2005,127(20):7312-7313
(Amino)(silyl)carbenes, prepared by substitution reactions at a carbene center, can survive several days at 0 degrees C. These species are not push-pull carbenes as their phosphino analogues and therefore are excellent ligands for transition-metal centers. 相似文献
64.
Wang Mei Miguel Daniel Riera Víctor Bois Claudette Jeannin Yves 《Transition Metal Chemistry》2001,26(4-5):566-569
A novel dimolybdenum complex [(3-C3H5)(CO)2Mo(-S2CPCy3)Mo(3-CH2CMeCH2)(CO)2], obtained by reacting the [(CO)2(3-C3H5)Mo(-S2CPCy3)Mo(CO)3]– anion with an excess of ClCH2CMe=CH2, has been characterized by i.r., 31P{1H}, 1H- and 13C-n.m.r. spectroscopy and by elemental analysis. The crystal structure of the complex, determined by X-ray diffraction, shows a definite preference for the central carbon of the S2CPCy3 bridge to bind to the Mo(2) atom coordinated by 3-2-methylallyl, rather than the Mo(1) atom attached to unsubstituted 3-allyl ligand. 相似文献
65.
(1S, 4R, 5S, 6S)-5-exo, 6-exo-(Isopropylidenedioxy)-7-oxabicyclo[2.2.1]heptan-2-one ((?)- 1 ) was transformed with high stereoselectivity to L -allose. Similarly, enantiomer (+)- 1 was transformed into L -talose. The ketones (+)- 1 and (?)- 1 were derived from furan and 1-cyanovinyl (1S)-camphanate and 1-cyanovinyl (1R)-camphanate, respectively. 相似文献
66.
Lemaître F Lucas D Groison K Richard P Mugnier Y Harvey PD 《Journal of the American Chemical Society》2003,125(18):5511-5522
The stoichiometric and catalytic activations of alkyl halides and acid chlorides by the unsatured Pd(3)(dppm)(3)(CO)(2+) cluster (Pd(3)(2+)) are investigated in detail. A series of alkyl halides (R-X; R = t-Bu, Et, Pr, Bu, allyl; X = Cl, Br, I) react slowly with Pd(3)(2+) to form the corresponding Pd(3)(X)(+) adduct and "R(+)". This activation can proceed much faster if it is electrochemically induced via the formation of the paramagnetic species Pd(3)(+). The latter is the first confidently identified paramagnetic Pd cluster. The kinetic constants extracted from the evolution of the UV-vis spectra for the thermal activation, as well as the amount of electricity to bring the activation to completion for the electrochemically induced reactions, correlate the relative C-X bond strength and the steric factors. The highly reactive "R(+)" species has been trapped using phenol to afford the corresponding ether. On the other hand, the acid chlorides react rapidly with Pd(3)(2+) where no induction is necessary. The analysis of the cyclic voltammograms (CV) establishes that a dissociative mechanism operates (RCOCl --> RCO(+) + Cl(-); R = t-Bu, Ph) prior to Cl(-) scavenging by the Pd(3)(2+) species. For the other acid chlorides (R = n-C(6)H(13), Me(2)CH, Et, Me, Pr), a second associative process (Pd(3)(2+) + RCOCl --> Pd(3)(2+.....)Cl(CO)(R)) is seen. Addition of Cu(NCMe)(4)(+) or Ag(+) leads to the abstraction of Cl(-) from Pd(3)(Cl)(+) to form Pd(3)(2+) and the insoluble MCl materials (M = Cu, Ag) allowing to regenerate the starting unsaturated cluster, where the precipitation of MX drives the reaction. By using a copper anode, the quasi-quantitative catalytic generation of the acylium ion ("RCO(+)") operates cleanly and rapidly. The trapping of "RCO(+)" with PF(6)(-) or BF(4)(-) leads to the corresponding acid fluorides and, with an alcohol (R'OH), to the corresponding ester catalytically, under mild conditions. Attempts were made to trap the key intermediates "Pd(3)(Cl)(+)...M(+)" (M(+) = Cu(+), Ag(+)), which was successfully performed for Pd(3)(ClAg)(2+), as characterized by (31)P NMR, IR, and FAB mass spectrometry. During the course of this investigation, the rare case of PF(6)(-) hydrolysis has been observed, where the product PF(2)O(2)(-) anion is observed in the complex Pd(3)(PF(2)O(2))(+), where the substrate is well-located inside the cavity formed by the dppm-Ph groups above the unsatured face of the Pd(3)(2+) center. This work shows that Pd(3)(2+) is a stronger Lewis acid in CH(2)Cl(2) and THF than AlCl(3), Ag(+), Cu(+), and Tl(+). 相似文献
67.
Marie E Chevalier Y Brunel S Eydoux F Germanaud L Flores P 《Journal of colloid and interface science》2004,269(1):117-125
The mechanism of action of additives that control the sedimentation of paraffin crystals after their crystallization in model diesel oil has been studied by means of a new experimental approach. The chemical analysis of the crystals and detailed measurements of the sedimentation phenomenon give new insights into this complex process. Thus, the wax antisettling additives used for preventing wax crystal sedimentation adsorb at the surfaces of wax particles and provide them with enhanced colloidal stability. The settling rate is not related to the size of the crystals or the viscosity of the liquid medium, but to the ability of the additives to prevent the aggregation of wax crystals. The reported methodology makes it possible to investigate the fundamental mechanisms, but also to evaluate structure-activity relationships of the various additives used in the petroleum industry. 相似文献
68.
Dino L. Pisaniello Peter J. Nichols Yves Ducommun Andr E. Merhach 《Helvetica chimica acta》1982,65(3):1025-1028
The temperature- and pressure-dependent equilibria for the addition of an extra N, N-dimethylforrnamide (DMF) or trimethylphosphate (TMP) ligand onto [Nd (DMF)8]3+- and [Nd(TMP)6]3+-species respectively have been measured by visible spectrophotometry. Complementary NMR. studies on other lanthanide ions show a gradual shift in preference for the lower coordination number across the lanthanide series. 相似文献
69.
The synthesis of C8-glycomimetics is described from C2-symmetrical polyhydroxylated cyclooctenes derived from carbocyclisation of enantiomerically pure 1,9-dienes by ring closing metathesis. Their obtention notably involved either hydroboration followed by oxidation to carbasugars or to cyclooctanones then reductive amination, or formation of a cis-cyclic sulfate followed by successive introduction of an azido group, reduction and subsequent reductive amination. The biological activity of the C8-carbasugars and related aminocyclitols, analogous to voglibose, has been evaluated towards several commercially available glycosidases. 相似文献
70.
Constable EC Figgemeier E Housecroft CE Olsson J Zimmermann YC 《Dalton transactions (Cambridge, England : 2003)》2004,(13):1918-1927
The synthesis and electronic properties of dinuclear ([(bipy)2Ru(I)M(terpy)][PF6]4(bipy = 2,2'-bipyridine, terpy = 2,2':6',2'-terpyridine; M = Ru, Os)) and trinuclear ([[(bipy)2Ru(I)]2M][PF6]6 M = Ru, Os, Fe, Co) complexes bridged by 4'-(2,2'-bipyridin-4-yl)-2,2':6',2'-terpyridine (I) have been investigated and are compared with those of mononuclear model complexes. The electrochemical analysis using cyclic voltammetry and differential pulse voltammetry reveals that there are no interactions in the ground state between adjacent metal centres. However, there is strong electronic communication between the 2,2'-bipyridine and 2,2':6',2'-terpyridine components of the bridging ligand. This conclusion is supported by a step-by-step reduction of the dinuclear and trinuclear complexes and the assignment of each electrochemical process to localised ligand sites within the didentate and terdentate domains. The investigation of the electronic absorption and emission spectra reveals an energy transfer in the excited state from the terminating bipy-bound metal centres to the central terpy-bound metal centre. This indicates that the bridge is able to facilitate energy transfer in the excited state between the metal centres despite the lack of interactions in the ground state. 相似文献