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101.
Ader C Spoerner M Kalbitzer HR Brunner E 《The journal of physical chemistry. B》2007,111(10):2752-2757
Liquid-state 31P NMR spectroscopy is a well-established method for the study of guanine nucleotide-binding proteins (GNB proteins) such as the proto-oncogene Ras. Solid-state 31P NMR spectroscopy could meanwhile also be used to study microcrystalline samples of Ras as well as its partial loss-of-function mutants Ras(T35S) and Ras(T35A). However, solid-state NMR studies of the latter mutants in complex with effector molecules such as RalGDS or Raf kinase were so far prevented, since it has been impossible to crystallize these complexes yet. The aim of the present contribution is to make such complexes accessible to solid-state 31P NMR spectroscopy by the application of precipitation methods. The complex formed by Ras(T35S) and Raf kinase is preserved during precipitation. In contrast, the weakly bound complex of Ras(T35S) with RalGDS is dissociated or at least perturbed by the precipitation procedure. Solid-state 31P NMR experiments on precipitates of these complexes deliver spectra of high resolution and signal-to-noise ratio which allows the application of two-dimensional techniques. Precipitates prepared using polyethylene glycol 6000 (PEG) as precipitant were found to exhibit spectra of maximum resolution and signal-to-noise ratio. Interestingly, the 31P signal due to the alpha-phosphate of GppNHp bound to Ras(T35S) in crystalline samples or aged precipitates has a significantly different isotropic chemical shift than in the liquid state or in freshly prepared precipitates. This directly indicates that the crystal structure differs from the equilibrium solution structure at least in the neighborhood of the alpha-phosphate group. 相似文献
102.
Polyelectrolyte microcapsules composed by using the LbL technique on stabilized RBC as templates were coated with up to ten layer pairs of trypsin/PSS or trypsin/alginate. The trypsin layer growth was confirmed by particle electrophoresis, confocal laser scanning microscopy, flow cytometry, and protein determination according to Lowry. In the coating series with trypsin/PSS, the amount of immobilized enzyme was larger than that with trypsin/alginate. The enzyme immobilization led to activity reduction of up to 90% compared to that of the same enzyme amount in the solution. No significant differences between the activities of trypsin immobilized in combination with PSS and with alginate were found. 相似文献
103.
Hydrogen bonding of the type SiO-H...A (A = O, N) has been studied in the gas phase for simple H3SiOH.acceptor complexes with the acceptor molecules being O(H)SiH3, OH2, O(H)CH3, O(CH3)2, O(CH3)SiH3, O(SiH3)2, NH3, N(CH3)H2, N(CH3)2H, N(CH3)3, N(CH3)2C6H5, and NC5H5, respectively, at the B3LYP/6-311+(2d,p) level of theory, using Bader's atoms in molecules (AIM) and Weinhold's natural bond orbital (NBO) methodology. For all complexes (except H3SiOH.N(CH3)2C6H5) the complex energy Eadd. is a good estimate for the hydrogen bond energy EHB, which is generally higher in N-acceptor complexes (-5.52 to -7.17 kcal mol-1) than in O-acceptor complexes (-2.09 to -5.06 kcal mol-1). In case of H3SiOH.N(CH3)2C6H5, EHB and Eadd. differ by the energy associated with the loss of n(N)-->pi conjugation in N(CH3)2C6H5 upon complex formation. EHB shows no correlation with O...A distances and the red shifts Deltanu(OH) of the OH-stretching vibrations when different acceptors are compared, although both parameters are commonly used to estimate the strength of the hydrogen bond from spectroscopic and diffraction data. A good linear correlation of the hydrogen bond energy EHB has been established with parameters derived from the AIM and NBO analyses, namely, the electron densities rho(HA) and rho(OH) at the H...A and O-H bond critical points (BCPs) and the NLMO bond orders BONLMO(HA) of the H...A bonds of the H3SiOH.acceptor complexes as well as the change of natural charges DeltaqNPA(O) at the O-donor atom upon H3SiOH.acceptor complex formation. Hydrogen bonding of the type SiO-H...A (A = O, N) has been also studied in the related cyclic multiple H3SiOH.acceptor complexes (H3SiOH)3, (H3SiOH)2.NC5H5, and (H3SiOH)4, respectively, at the same level of theory. Cooperative hydrogen bonding is evident for all cyclic multiple H3SiOH.acceptor complexes, whereby the strongest concomitant strengthening of the hydrogen bonds is observed for (H3SiOH)4 and (H3SiOH)2.NC5H5. 相似文献
104.
Chlorination of bis(supermesityl)ditelluride RTeTeR (R = 2,4,6-t-Bu3C6H2) with 3 equiv of sulfuryl chloride SO2Cl2 provided the intrinsically unstable supermesityltellurium(IV) trichloride RTeCl3 (1) as bright yellow crystals. Severe repulsion between the equatorial Cl atom and one tert-butyl group in an ortho position in the supermesityl ligand is the reason for the extreme reactivity of 1, which is in contrast to that of all previously known monoorganotellurium trihalides. In the solid state at room temperature, (the triclinic modification of) 1 reacts slowly under HCl elimination and intramolecular Te-C bond formation to give the bicyclic 5,7-di-tert-butyl-2-hydro-3,3-dimethylbenzo[b]tellurophene-1,1-dichloride (2), which was originally obtained as a colorless amorphous solid. On one occasion, when the solid-state reaction was allowed to occur under air conditions, compound 2 and a colorless crystalline byproduct, namely, trans-supermesityltellurium hydroxide dichloride (3), had formed, from which a few crystals were hand-selected. The formation of 3 has been tentatively rationalized by a solid-state hydrolysis of a second (monoclinic?) modification present in the bulk material of 1. In diethyl ether, THF, or carbon disulfide, a redox equilibrium exists between yellow supermesityltellurium(IV) trichloride RTeCl3 (1), deep blue supermesityltellurenyl(II) chloride RTeCl (4), and chlorine gas, which can be shifted to 4 when the reaction vessel is purged with argon to remove the chlorine gas. Compound 4 was also obtained by the reaction of RTeTeR (R = 2,4,6-t-Bu3C6H2) with 1 equiv of SO2Cl2. When a solution of 1 was stored with an excess of SO2Cl2 for a prolonged amount of time, Te-C bond cleavage occurred and [(Et2OH)2Te2Cl10].2Et2O (5) was formed. Compounds 1-5 have been characterized by X-ray crystallography. 相似文献
105.
The single‐crystal X‐ray structure analysis of hexakis(2,4,6‐triisopropylphenyl)cyclotristannoxane, cyclo‐[(2,4,6‐i‐Pr3‐C6H2)2SnO]3 ( 1 ), is reported and reveals this compound to contain an almost planar six‐membered ring. Redistribution reactions of 1 with cyclo‐(t‐Bu2SnO)3 and t‐Bu2SiCl2, respectively, failed and indicate an unusual kinetic inertness of the Sn–O bonds in 1 as compared to related molecular diorganotin oxides containing less bulkier substituents. The redistribution reaction of cyclo‐(t‐Bu2SnO)3 with cyclo‐(t‐Bu2SnS)2 leads to an equilibrium involving the trimeric diorganotin oxysulphides cyclo‐t‐Bu2Sn(OSnt‐Bu2)2S ( 2 a ) and cyclo‐t‐Bu2Sn(SSnt‐Bu2)2O ( 2 b ). 相似文献
106.
Jens Beckmann Klaus Jurkschat Stephanie Rabe Markus Schürmann Dainis Dakternieks 《无机化学与普通化学杂志》2001,627(3):458-464
The syntheses of the asymmetrically substituted tetraorganodistannoxanes [t‐Bu2(X)SnOSn(Y)(CH2SiMe3)2]2 ( 1 , X = Y = OH; 2 , X = Cl, Y = OH; 3 , X = Y = Cl) are reported and their structures in solution and in the solid state are characterized by multinuclear NMR spectroscopy and single crystal X‐ray analyses. In toluene, the tetrahydroxy‐substituted derivative 1 is in equilibrium with the organotin oxides cyclo‐[t‐Bu2Sn{OSn(CH2SiMe3)2}2O] ( 4 ), cyclo[(Me3SiCH2)2Sn(OSnt‐Bu2)2O] ( 5 ), and cyclo‐(t‐Bu2SnO)3, and some additional, undefined species containing pentacoordinated tin atoms. In contrast, the dihydroxydichloro‐substituted derivative 2 is inert in solution. 相似文献
107.
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110.
Adrian E. Ion Eike T. Spielberg Lorenzo Sorace Axel Buchholz Winfried Plass 《Solid State Sciences》2009,11(4):766-771
Reaction of the copper precursor [Cu(MeOsaltn)(H2O)] (H2MeOsaltn = N,N′-bis(3-methoxysalicylidene)-1,3-diaminopropane) with Ln(NO3)3·6H2O (Ln = Sm and Tb) and pyrazine-2,3-dicarboxylic acid (H2pyrdic) results in the formation of 1D zigzag chains with the general formula of [Cu(MeOsaltn)Ln(NO3)(pyrdic)]n·nDMF. X-ray crystal structures reveal that the samarium and terbium compounds are isostructural and crystalize in the orthorhombic space group Pbcn. The chains are composed of heterodinuclear copper–lanthanide building blocks which are linked by the pyrazine-2,3-dicarboxylate bridging units. Temperature-dependent susceptibility measurements indicate antiferromagnetic exchange interactions for the samarium–copper chain whereas for the terbium–copper compound ferromagnetic interactions are observed. 相似文献