排序方式: 共有18条查询结果,搜索用时 15 毫秒
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H. Mühe Mc. Candless E. Valenta Utz Wilh Vaubel B. Ahlström O. Aschan J. Kondakow J. Schindelmeiser R. Böhme H. Herzfeld J. E. Teeple R. Adan J. Marcusson Darmois H. Wolff C. Piest R. Marcille EA. Parry M. Adams H. W. Fosse K. Ihnatowzcz 《Analytical and bioanalytical chemistry》1917,56(10-11):541-560
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RD Harris WS Baker Van Stipdonk MJ RM Crooks EA Schweikert 《Rapid communications in mass spectrometry : RCM》1999,13(14):1374-1380
A suite of keV polyatomic or 'cluster' projectiles was used to bombard unoxidized and oxidized self-assembled monolayer surfaces. Negative secondary ion yields, collected at the limit of single ion impacts, were measured and compared for both molecular and fragment ions. In contrast to targets that are orders of magnitude thicker than the penetration range of the primary ions, secondary ion yields from polyatomic projectile impacts on self-assembled monolayers show little to no enhancement when compared with monatomic projectiles at the same velocity. This unusual trend is most likely due to the structural arrangement and bonding characteristics of the monolayer molecules with the Au(111). Copyright 1999 John Wiley & Sons, Ltd. 相似文献
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Aderholz M Aggarwal MM Akbari H Allport PP Badyal SK Ballagh HC Barth M Baton JP Bingham HH Brucker EB Burnstein RA Campbell JR Cence RJ Chatterjee TK Clayton EF Corrigan G Coutures C DeProspo D Devanand De Wolf EA Faulkner PJ Foeth H Fretter WB Gupta VK Hanlon J Harigel G Harris FA Jabiol MA Jacques P Jain V Jones GT Jones MD Kafka T Kalelkar M Kasper P Kohli JM Koller EL Krawiec RJ Lauko M Lys JE Marage P Milburn RH Miller DB Mittra IS Mobayyen MM Moreels J Morrison DR Myatt G Nailor P 《Physical review D: Particles and fields》1992,45(7):2232-2243
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As part of our search for photoactive ruthenium nitrosyls, a set of {RuNO}6 nitrosyls has been synthesized and structurally characterized. In this set, the first nitrosyl [(SBPy3)Ru(NO)](BF4)3 (1) is derived from a polypyridine Schiff base ligand SBPy3, while the remaining three nitrosyls are derived from analogous polypyridine ligands containing either one ([(PaPy3)Ru(NO)](BF4)2 (2)) or two ([(Py3P)Ru(NO)]BF4 (3) and [(Py3P)Ru(NO)(Cl)] (4)) carboxamide group(s). The coordination structures of 1 and 2 are very similar except that in 2, a carboxamido nitrogen is coordinated to the ruthenium center in place of an imine nitrogen in case of 1. In 3 and 4, the ruthenium center is coordinated to two carboxamido nitrogens in the equatorial plane and the bound NO is trans to a pyridine nitrogen (in 3) and chloride (in 4), respectively. Complexes 1-3 contain N6 donor set, and the NO stretching frequencies (nuNO) correlate well with the N-O bond distances. All four diamagnetic {RuNO}(6) nitrosyls are photoactive and release NO rapidly upon illumination with low-intensity (5-10 mW) UV light. Interestingly, photolysis of 1 generates the diamagnetic Ru(II) photoproduct [(SBPy3)Ru(MeCN)](2+) while 2-4 afford paramagnetic Ru(III) species in MeCN solution. The quantum yield values of NO release under UV illumination (lambda(max) = 302 nm) lie in the range 0.06-0.17. Complexes 3 and 4 also exhibit considerable photoactivity under visible light. The efficiency of NO release increases in the order 2 < 3 < 4, indicating that photorelease of NO is facilitated by (a) the increase in the number of coordinated carboxamido nitrogen(s) and (b) the presence of negatively charged ligands (like chloride) trans to the bound NO. 相似文献