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111.
Unraveling of all of the information contained in proteomes poses a tremendous chemical challenge, which is balanced by the promise of potentially transformational knowledge. Mass spectrometry offers an unprecedented arsenal of tools for diverse proteomic investigations. Recently, it was demonstrated that ultraviolet light can be utilized to initiate unique and potentially useful fragmentations in peptides and proteins. Either nonspecific dissociation or highly specific dissociation at engineered chromophoric sites is possible following photon absorption. The level of specificity and control over fragmentation in these experiments is greater than with other fragmentation methods. Novel techniques made possible by this technology are poised to make substantial contributions to the field of proteomics. 相似文献
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Bravo-Castillero Julian; Rodriguez-Ramos Reinaldo; Mechkour Houari; Otero Jose A.; Sabina Federico J. 《The Quarterly Journal of Mechanics and Applied Mathematics》2008,61(3):311-332
In this work, based on the periodic unfolding homogenizationtechnique, the limiting equations modelling the behaviour ofthree-dimensional magneto-electro-elastic periodic structuresare rigorously established. The local problems and the correspondinghomogenized coefficients of the elastic, dielectric, magneticpermittivity, piezoelectric, piezomagnetic and magneto-electric(ME) tensors are explicitly described. The homogenization modelis exemplified for laminated composites and a unified generalformula for all effective properties of periodic multilaminatedmagneto-electro-elastic composites is obtained. This formulais applied to investigate the global behaviour for the importantcase of transversely isotropic constituents and any finite numberof layers in each periodic cell. Examples that provide theoreticalevidence of the presence of both a product property and theME effect are given. 相似文献
114.
Julian J. Adams David E. Berry Jane Browning Dirk Burth Owen J. Curnow 《Journal of organometallic chemistry》1999,580(2):6418
The preparation, isolation and characterisation of 1,3-bis(diphenylphosphino)indene (1) from indene and chlorodiphenylphosphine is described. The reaction of 1 with selenium gives the diselenide adduct 1,3-bis(diphenylselenophosphino)indene (2) which was characterised crystallographically. Deprotonation of 1 and treatment with ferrous chloride gives the unstable tetraphosphine complex bis(1,3-bis(diphenylphosphino)indenyl)iron(II) (3). Complex 3 decomposes to the diphosphine complex bis(1-diphenylphosphinoindenyl)iron(II) (4) via replacement of one diphenylphosphine substituent per indenyl ligand by a hydrogen atom. Complex 4 was also prepared by treatment of two equivalents of 1-diphenylphosphinoindenide with ferrous chloride. The heterobimetallic complex tetracarbonyl(bis(1-diphenylphosphinoindenyl)iron(II))molybdenum(0) (5) was also prepared and crystal structures of both the meso (5a) and C2-symmetric racemic (5b) isomers are reported. 相似文献
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Rishav Choudhary Julian J. Girard Sean Clees Sarah E. Johnson Jiankun Shao David F. Davidson Ronald K. Hanson Allen A. Aradi 《Proceedings of the Combustion Institute》2021,38(1):957-965
We report the first shock tube measurements of formaldehyde (CH2O) during the first stage ignition of n-heptane, 2-methylhexane and 3,3-dimethylpentane, in highly diluted fuel/oxygen mixtures in the pressure range of 7–10 atm and temperature range of 700–880 K. Combined time histories of all carbonyl (–C = O) species, CO and fuel were also measured simultaneously in an effort to study the impact of fuel structure on the concentration and the rate of evolution of first stage ignition products. Of the three isomers studied in this work, n-heptane was found to be the fastest, while 3,3-dimethylpentane was found to be the slowest. The differences in the time scale of formation, and plateau concentration of the intermediates between the isomers across the entire range of test conditions suggests a strong dependency of the measured time histories to fuel structure. These species therefore act as markers of the Negative Temperature Coefficient (NTC) behavior of fuels and can be used as targets for developing semi-empirical, hybrid chemistry models of complex, multi-component petroleum derived gasoline and jet fuels. The time histories reported in this work should prove very useful in the refinement of detailed kinetic models of n-heptane, and development of rate rules for branched alkane isomers. 相似文献
120.
Sergey Miltsov Vladimir Karavan Alexandr Misharev Galina Starova Julian Alonso-Chamarro Mar Puyol 《Tetrahedron letters》2017,58(34):3353-3357
meso-Bromosubstituted indodicarbocyanine dyes produce dimeric molecules, together with the debrominated species, under acid catalysis. The relationship between the dimerization and hydrodebromination routes depends on the aryl substitution of the dyes. A possible reaction mechanism is also proposed. 相似文献