排序方式: 共有90条查询结果,搜索用时 15 毫秒
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Adler J Becker JJ Blaylock GT Bolton T Brown JS Bunnell KO Burnett TH Cassell RE Coffman D Cook V Coward DH Dorfan DE Dubois GP Duncan AL Eigen G Einsweiler KF Eisenstein BI Freese T Gladding G Grab C Grancagnolo F Hamilton RP Hauser J Heusch CA Hitlin DG Izen JM Köpke L Li A Lockman WS Mallik U Matthews CG Mir R Mockett PM Mozley RF Nemati B Odian A Parrish L Partridge R Perrier J Pitman D Plaetzer SA Richman JD Sadrozinski HF Scarlatella M Schalk TL Schindler RH Seiden A Simopoulos C 《Physical review letters》1988,60(14):1375-1378
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We analyse different error propagation mechanisms for conservativeand nonconservative time-integrators of nonlinear Schrödingerequations. We use a geometric approach based on interpretingwaves as relative equilibria. 相似文献
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Bai JZ Bardon O Becker-Szendy RA Blum I Breakstone A Burnett T Chen GP Chen HF Chen J Chen SJ Chen SM Chen Y Chen YB Chen YQ Cheng BS Cowan RF Cui HC Cui XZ Ding HL Du ZZ Dunwoodie W Fan XL Fang J Gao CS Gao ML Gao SQ Gao WX Gratton P Gu JH Gu SD Gu WX Gu YF Guo YN Han SW Han Y Harris FA Hatanaka M He J He KR He M Hitlin DG Hu GY Hu T Hu XQ Huang DQ Huang YZ Izen JM Jia QP Jiang CH Jiang ZZ Jin S Jin Y Jones L Kang SH Ke ZJ Kelsey MH Kim BK Lai YF Lan HB Lang PF Lankford A Li F Li J Li PQ 《Physical review D: Particles and fields》1996,53(1):20-34
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Coffman D DeJongh F Dubois GP Eigen G Hitlin DG Matthews CG Mincer A Richman J Weinstein AJ Wisniewski WJ Zhu Y Bolton T Bunnell KO Cassell RE Coward DH Kim PC Labs J Odian A Pitman D Schindler RH Toki W Wasserbaech S Drinkard JJ Gatto C Heusch CA Lockman WS Scarlatella M Sadrozinski HF Schalk TL Seiden A Weseler S Eisenstein BI Freese T Gladding G Izen JM Stockdale IE Tripsas B Mallik U Wang MZ Brown J Burnett TH Li AD Mir R Mockett PM Nemati B Parrish L Willutzki H 《Physical review D: Particles and fields》1992,45(7):2196-2211
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Adler J Becker JJ Blaylock GT Bolton T Brown JS Bunnell KO Burnett TH Cassell RE Coffman D Cook V Coward DH Dorfan DE Dubois GP Duncan AL Eigen G Einsweiler KF Eisenstein BI Freese T Gladding G Grab C Grancagnolo F Hamilton RP Hauser J Heusch CA Hitlin DG Izen JM Köpke L Li A Lockman WS Mallik U Matthews CG Mir R Mockett PM Mozley RF Nemati B Odian A Parrish L Partridge R Perrier J Pitman D Plaetzer SA Richman JD Sadrozinski HF Scarlatella M Schalk TL Schindler RH Seiden A Simopoulos C 《Physical review letters》1987,59(14):1527-1529
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Successive oxidation of transition metal(II) aqua complexes (M(II)OH(2) to M(III)OH) is a domain in which proton-coupled electron transfer reactions are extremely common. The mechanism of these PCET reactions-concerted or stepwise-is an important issue in the understanding and design of natural or artificial systems catalyzing the formation of dioxygen by four-electron oxidation of water. Concerted proton-coupled electron transfer from an aqua metal(II) to a hydroxo metal(III) complex requires the close proximity of a proton-accepting group with a pK value between those of the aqua complexes. Otherwise, stepwise electron-proton or proton-electron pathways involving high-energy intermediates are followed. Concerted proton-electron pathways involving water as proton-acceptor or proton-donor group are inefficient. Cyclic voltammetry of the title complex in buffered aqueous solution and re-examination of previous results for the same complex attached to an electrode surface are used to establish these conclusions, which provide a starting point on the route to higher degrees of oxidation, such as those involved in the catalysis of water oxidation. 相似文献
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