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1.
We comment on a recent paper [J Opt Laser Technol 43 (2011) 430–436] in which the authors introduce dispersion and attenuation models of spatially multiplexed channels in step index multimode fibers. We consider the theoretical explanation of the model given in the paper incorrect. 相似文献
2.
I. Garcia V. Uc M. E.Ruiz Y. G. Smeyers A. Vivier Bunge 《Journal of Molecular Structure》1995,340(1-3):149-158
Unrestricted Hartree-Fock calculations have been carried out to study the benzylperoxyl radical, an intermediate atmospheric contaminant. For this purpose, quantum mechanical MP2//UHF ab initio calculations were performed by using 6-31G** and 6-31 + G** basis sets. Because no previous experimental nor theoretical data were available for benzylperoxyl, the results were compared with those of the smaller unsaturated peroxyl radicals, such as allylperoxyl. It is found that the calculated absolute minimal energy corresponds to a trans conformation in which the O---O bond is sticking away from the benzene ring. Benzylperoxyl is found also to exhibit an unusually O---O small bond order, which reflects the weakness of the bond, i.e. its ability to react with NO forming NO2 and subsequently ozone. A peculiar MO diagram is obtained, with the unpaired MO deeply located in the “doubly” occupied MO space. This effect is also observed in allylperoxyl. Structural parameters, charges, spin densities and dipole moments are also reported. 相似文献
3.
Evgeny M. Garanin Yuriy V. Tolmachev Scott D. Bunge Anatoly K. Khitrin Alexander N. Turanov Andrey Malkovskiy Alexei P. Sokolov 《Journal of Solid State Electrochemistry》2011,15(3):549-560
We report on the crystal structures of two hydrates of benzenehexasulfonic acid, its water sorption isotherm, temperature- and humidity-dependent conductivity, along with 1H NMR studies. At comparable humidities and temperatures, this crystalline material shows conductivity similar to Nafion, which conducts protons via liquid water channels. We believe that the presented discovery of fast protonic conductivity in benzenehexasulfonic acid at low humidities is encouraging for further efforts in developing highly sulfonated polymers as membranes for fuel cells. 相似文献
4.
5.
Heinz Nadig Urs Squin Richard H. Bunge Timothy R. Hurley David B. Murphey James C. French 《Helvetica chimica acta》1985,68(4):953-957
A novel antibiotic, PD 121,222, was isolated from a complex of pluramycin-like compounds containing mostly kidamycin and neopluramycin. Spectral analyses showed that this compound is the 14,16-dihydroxy analog of rubiflavin A. 相似文献
6.
7.
Generation and NMR studies of novel carbocations and carboxonium ions are reported from sterically hindered stilbene 1,1'-bi(benzocyclobutenylidene) 1, its dimethoxy derivative 5, and from their skeletally rearranged derivatives, namely, the spirocyclic ketone 6, diastereomeric alcohols 7 and isomeric diols 8. Quenching experiments on the carbocations under various conditions resulted in the formation/isolation of several novel covalent adducts. Acid-catalyzed isomerization of the diols 8 produced a remarkable dimeric molecule, whose structure was confirmed by X-ray analysis. Reactions of hindered stilbenes 1 and 5 with Br 2/CDCl 3 were examined via NMR experiments. The experimentally observed carbocations were also studied computationally by GIAO-DFT and by NICS. 相似文献
8.
Boyle TJ Sewell RM Ottley LA Pratt HD Quintana CJ Bunge SD 《Inorganic chemistry》2007,46(5):1825-1835
The reaction of [Ti(mu-ONep)(ONep)3]2 (ONep = OCH2C(CH3)3) with a series of heterocyclic methanol derivatives [tetrahydrofurfuryl alcohol (H-OTHF), thiophene methanol (H-OTPM), or 2-pyridylcarbinol (H-OPy)-collectively termed H-OR*], led to the isolation of a novel family of OR*-substituted titanium alkoxide precursors. Independent of the initial stoichiometry for the H-OTHF reaction, a monosubstituted, dinuclear species was isolated as [(ONep)3Ti(muc-OTHF)]2 (1). For 1, each Ti was octahedrally (Oh) bound by three terminal ONep ligands, one bidentate bridging OTHF ligand (muc-OTHF), and an oxygen from the other muc-OTHF ligand. For the OTPM derivatives, the product was identified as [(ONep)3Ti(mu-OTPM)]2 (2). For this ligand, the soft S atom does not bind to the Ti but the O atom does act as a bridge between the two trigonal bipyramidal bound Ti metal centers. The OPy system yielded (OPy)2Ti(OR)2 independent of the OR and the stoichiometry used [OR = ONep (3), OCHMe2 (4), OCMe3 (5)]. For 3-5, the two OPy ligands chelate to the Oh-bound Ti metal center with two terminal OR ligands. Compounds 1-5 were fully characterized using a variety of analytical techniques. An initial investigation of the proposed chemical stability of the '(OPy)2Ti' moiety of 3-5 to alcoholysis exchange pathways involving (i) alkyl alcohols, (ii) aryl alcohols, (iii) substituted phenols, (iv) H-OR* derivatives, and (v) silanols proved successful through the isolation of a novel family of structurally characterized (OPy)2Ti(OR')2 (7-24) compounds. 相似文献
9.
Hannibal L Bunge SD van Eldik R Jacobsen DW Kratky C Gruber K Brasch NE 《Inorganic chemistry》2007,46(9):3613-3618
The X-ray structures of imidazolylcobalamin (ImCbl) and histidinylcobalamin (HisCbl) are reported. These structures are of interest given that the recent structures of human and bovine transcobalamin prepared in their holo forms from aquacobalamin show a histidine residue of the metalloprotein bound at the beta-axial site of the cobalamin (Wuerges, J. et al. Proc. Natl. Acad. Sci. U.S.A. 2006, 103, 4386-4391). The beta-axial Co-N bond distances for ImCbl and HisCbl are 1.94(1) and 1.951(7) A, respectively. The alpha-axial Co-N bond distances to the 5,6-dimethylbenzimidazole are 2.01(1) and 1.979(8) A for ImCbl and HisCbl, respectively, and are typical for cobalamins with weak sigma-donor ligands at the beta-axial site. The corrin fold angles of 11.8(3) degrees (ImCbl) and 12.0(3) degrees (HisCbl) are smaller than those typically observed for cobalamins. 相似文献
10.
The reaction of 1,1,3,3-tetramethylguanidine (HTMG) with [UO(2)Cl(2)(THF)2] yielded [UO(2)Cl(2)(HTMG)2] 1, the first uranyl tetralkylguanidine adduct reported, further investigation led to the synthesis of [UO(2)(DBP)2(HTMG)2] 2 and [UO(2)(DBP-4-Me)2(HTMG)2] 3 via the reaction of [UO(2){N(SiMe(3))2}2(THF)2] with HTMG and the appropriate aryl alcohol, HO-2,6-(t)Bu(2)-4-RC(6)H(2) (R = H, DBP; R = CH(3), DBP-4-Me). 相似文献