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231.
Konstantinos A. Lazarou Karilys Gonzlez‐Nieves Indranil Chakraborty Raphael G. Raptis 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(22):7402-7406
The P and M enantiomers of the octanuclear [Fe8(μ4‐O)4(μ‐4‐Cl‐pz)12Cl4] complex, having T symmetry, were resolved by temporary substitution of chloride ligands by racemic 4‐sBu‐phenolates and subsequent crystallization, where the (S)‐ and (R)‐phenolates coordinate selectively to the M and P complexes, respectively. The complexes were characterized by circular dichroism analysis and X‐ray structure determination. This work constitutes a rare example of enantiomeric recognition resulting in spontaneous resolution upon crystallization. 相似文献
232.
Dubroka A Kim KW Rössle M Malik VK Drew AJ Liu RH Wu G Chen XH Bernhard C 《Physical review letters》2008,101(9):097011
We present far-infrared ellipsometric measurements of polycrystalline samples of the pnictide superconductor RFeAsO0.82F0.18 (R=Nd and Sm). We find evidence that the electronic properties are strongly anisotropic such that the optical spectra are dominated by the weakly conducting c-axis response similar to the cuprate high-temperature superconductors. We deduce an upper limit of the c-axis superconducting plasma frequency of omega pl,c(SC)< or =260 cm(-1) corresponding to a lower limit of the c-axis magnetic penetration depth of lambda c > or =6 microm and lambda c/lambda ab > or =30 as compared to lambda ab=185 nm from muon spin rotation [A. Drew, arXiv:0805.1042 [Phys. Rev. Lett. (to be published)]]. We also observe a gaplike suppression of the conductivity in the superconducting state with a shoulderlike feature at omegaSC* approximately 300 cm(-1) and spectral shape which is consistent with an unconventional order parameter with 2Delta approximately omegaSC* approximately 37 meV. 相似文献
233.
Sutapa Sen Manas K. Saha Tarakranjan Gupta Aswini K. Karmakar Parimal Kundu Samiran Mitra Michael B. Hursthouse K. M. Abdul Malik 《Journal of chemical crystallography》1998,28(10):771-777
The compound [Cu(phen)(O2CCF3)2]n (phen = 1,10-phenanthroline) has been synthesized and its crystal structure determined. It crystallizes in monoclinic space group C2/c, with a = 19.229(7), b = 11.281(5), c = 7.621(2) Å, = 104.305(12)°, and Z = 4. The crystal structure is polymeric, being built from infinite zigzag chains of trifluoroacetate bridged copper(II), with the phenanthroline ligands being stacked between the chains. The variable-temperature (13–300 K) magnetic susceptibility and ESR data are reported and a weak ferromagnetic exchange interaction is observed with the exchange parameter estimated as J = 2.9 cm–1. 相似文献
234.
Ananta Karmakar Mushkin Basha G.T. Venkatesh Babu Murali Botlagunta Noormohamed Abdul Malik Richard Rampulla Arvind Mathur Arun Kumar Gupta 《Tetrahedron letters》2018,59(48):4267-4271
A number of cyanomethyl esters of natural/unnatural aminoacids with un-protected amino functionality were synthesized because of their synthetic and medicinal importance. Critical N-Boc deprotection methods in the presence of labile (hydrolytic sensitivity) cyanomethyl functionality were screened thoroughly and it was found that readily available 4M HCl in 1,4-dioxane solution (2–4 equiv); acetonitrile, 0?°C, 2–4?h was a suitable condition. This condition was generalized and successfully applied to a variety of alkyl, alkynyl, aryl, heteroaryl, benzyl, azido, spiro amino acid cyanomethylesters irrespective of the nature of the amine (primary or secondary) and the distance between the amine and ester group to achieve final deprotected amino esters with high yield, and purity compared to other commonly known N-protecting groups (Cbz, Fmoc, Ac, Bn, Bz etc.). It was also demonstrated that N-Boc protected aminoacid cyanomethylesters are stable enough to carry out further functionalization compared to N-unprotected counterparts. 相似文献
235.
Gulshan Ara Shariff E. Kabir Kalipada Kundu K. M. Abdul Malik 《Journal of chemical crystallography》2003,33(11):851-857
The dimeric complex [Mn2(-pyS)2(CO)6] (1) reacted with 2 equivalents of 2,2-bipyridyl (bipy), 1,10-phenanthroline (phen), and ethylenediamine (en) to give the corresponding monomeric complexes [Mn(1-pyS)(bipy)(CO)3] (2), [Mn(1-pyS)(phen)(CO)3] (3), and [Mn( 1-pyS)(en)(CO)3] (4). The pyS ligand in these complexes acts as a monodentate, two-electron donor ligand, which coordinates to manganese through the sulfur atom. This is confirmed by an X-ray structure determination of 2, which contains two structural isomers in the asymmetric unit. Crystals of this compound are the monoclinic, space group P2
1/c, a = 21.593(4), b = 10.463(2), c = 16.385(3) Å, = 102.468(13)°, V = 3614.5(12) Å3, and Z = 8. The three CO groups are facially distributed in both isomers, but the relative positions of the pyS and bipy ligands are different. 相似文献
236.
Stephen J. Sweetman Charles D. Immanuel Tahir I. Malik Simon Emmett Neal Williams 《大分子反应工程》2008,2(5):382-397
A sensitivity study of particle size distribution (PSD) and molecular weight distribution (MWD) responses to perturbations in initiator, surfactant, monomer and chain transfer agent in a semi‐batch emulsion polymerisation is presented. The objective is to provide a systematic study on the ability to simultaneously control both PSD and MWD, towards inferential control of end‐use product properties. This would lead towards identification of the practical feasible regions of operability. All inputs appeared to have an intrinsic and simultaneous influence on end‐time PSD and MWD. Trends shown in experimental results have been explained in a mechanistic sense and also compared to simulation results from a combined PSD/MWD population balance model. The preliminary comparison between experiment and simulation highlights areas to be focussed on with respect to model improvement.
237.
Indranil Biswas 《Bulletin des Sciences Mathématiques》2008,132(1):1
Let C be an irreducible smooth projective curve defined over an algebraically closed field k. Let G be a semisimple linear algebraic group defined over the field k and P⊂G a proper parabolic subgroup. Fix a strictly anti-dominant character χ of P. Let EG be a semistable principal G-bundle over C. If the characteristic of k is positive, then EG is assumed to be strongly semistable. Take any real number ?>0. Then there is an irreducible smooth projective curve defined over k, a nonconstant morphism
238.
Bartoli S Mahmood T Malik A Dixon S Kilburn JD 《Organic & biomolecular chemistry》2008,6(13):2340-2345
A chiral bisguanidinium macrocycle binds N-Boc-L-glutamate in a 1 : 1 stoichiometry with significant selectivity in competitive solvent (DMSO-H(2)O). 相似文献
239.
The addition of cationic surfactant, cetlytrimethylammoniumbromide (CTAB), in benzene and aqueous potassium permanganate solution brought the MnO from the aqueous phase to the organic phase. At 525 nm, the absorbance of the organic phase increased until it reached a maximum, and then decreased with [CTAB]. The effect of [CTAB] on the reduction of permanganate by D ‐glucose in a benzene–CTAB system has been studied spectrophotmetrically. The observed effect on the rate constant is catalytic up to a certain concentration of CTAB; thereafter, a saturation phenomenon is observed with an increased concentration of CTAB. The oxidation reaction obeyed the first‐order kinetics with respect to the D ‐glucose. On addition of H2SO4, there was a decrease in the rate constants. There is evidence for the existence of manganese as a water‐soluble colloidal MnO2. A detailed mechanism with the associated reaction kinetics is presented and discussed. © 2008 Wiley Periodicals, Inc. 40: 496–503, 2008 相似文献
240.
One-dimensional hydrogen-bonded complex [Zn(bpe)(2)(H(2)O)(4)](NO(3))(2).8/3 H(2)O.2/3 bpe (1, bpe=4,4'-bipyridylethylene) containing coordination complex cations [Zn(bpe)(2)(H(2)O)(4)](2+) with parallel and crisscross double bonds undergoes photochemical [2+2] cycloaddition in the solid state and produces tetrakis(4-pyridyl)cyclobutane (tpcb) in up to 100 % yield with rctt-tpcb (2a) as major and rtct-tpcb (2b) as minor product. The bpe ligands with crisscross conformation of C=C bonds appear to undergo pedal-like motion prior to photodimerization. Grinding single crystals to powder accelerates the pedal motion of crisscrossed olefins in the bpe ligands to parallel alignment and provides the rctt-cyclobutane stereoisomer 2a quantitatively. In addition, 100 % photodimerization of ground 1 indicates that the free bpe ligands, which are remote from each other in a pool of water, and NO(3)(-) ions moved toward each other to give a mixture of rctt- and rtct-tpcb isomers. 相似文献