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排序方式: 共有66条查询结果,搜索用时 15 毫秒
1.
Alexopoulos T Allen C Anderson EW Areti H Banerjee S Beery PD Biswas NN Bujak A Carmony DD Carter T Cole P Choi Y De Bonte RJ Erwin AR Findeisen C Goshaw AT Gutay LJ Hirsch AS Hojvat C Kenney VP Lindsey CS LoSecco JM McMahon T McManus AP Morgan N Nelson KS Oh SH Piekarz J Porile NT Reeves D Scharenberg RP Stampke SR Stringfellow BC Thompson MA Turkot F Walker WD Wang CH Wesson DK 《Physical review letters》1990,64(9):991-994
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Jacobi BG Laitar DS Pu L Wargocki MF DiPasquale AG Fortner KC Schuck SM Brown SN 《Inorganic chemistry》2002,41(18):4815-4823
Trimesityliridium(III) (mesityl = 2,4,6-trimethylphenyl) reacts with O(2) to form oxotrimesityliridium(V), (mes)(3)Ir=O, in a reaction that is cleanly second order in iridium. In contrast to initial reports by Wilkinson, there is no evidence for substantial accumulation of an intermediate in this reaction. The oxo complex (mes)(3)Ir=O oxidizes triphenylphosphine to triphenylphosphine oxide in a second-order reaction with DeltaH++ = 10.04 +/- 0.16 kcal/mol and DeltaS++ = -21.6 +/- 0.5 cal/(mol.K) in 1,2-dichloroethane. Triphenylarsine is also oxidized, though over an order of magnitude more slowly. Ir(mes)(3) binds PPh(3) reversibly (K(assoc) = 84 +/- 3 M(-1) in toluene at 20 degrees C) to form an unsymmetrical, sawhorse-shaped four-coordinate complex, whose temperature-dependent NMR spectra reveal a variety of dynamic processes. Oxygen atom transfer from (mes)(3)Ir=O and dioxygen activation by (mes)(3)Ir can be combined to allow catalytic aerobic oxidations of triphenylphosphine at room temperature and atmospheric pressure with overall activity (approximately 60 turnovers/h) comparable to the fastest reported catalysts. A kinetic model that uses the rates measured for dioxygen activation, atom transfer, and phosphine binding describes the observed catalytic behavior well. Oxotrimesityliridium does not react with sulfides, sulfoxides, alcohols, or alkenes, apparently for kinetic reasons. 相似文献
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Lazarus EA Navratil GA Greenfield CM Strait EJ Austin ME Burrell KH Casper TA Baker DR DeBoo JC Doyle EJ Durst R Ferron JR Forest CB Gohil P Groebner RJ Heidbrink WW Hong R Houlberg WA Howald AW Hsieh C Hyatt AW Jackson GL Kim J Lao LL Lasnier CJ Leonard AW Lohr J La Haye RJ Maingi R Miller RL Murakami M Osborne TH Perkins LJ Petty CC Rettig CL Rhodes TL Rice BW Sabbagh SA Schissel DP Scoville JT Snider RT Staebler GM Stallard BW Stambaugh RD St John HE Stockdale RE Taylor PL Thomas DM 《Physical review letters》1996,77(13):2714-2717
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T. A. Furstch L. T. Taylor T. W. Fritz G. Fortner E. Khor 《Journal of polymer science. Part A, Polymer chemistry》1982,20(5):1287-1298
Five polyimide films prepared from 3,3′,4,4′-benzophenone tetracarboxylic acid'dianhydride (BTDA) and diamines, 4,4′-oxydianiline (ODA), 3,3′-diaminobenzophenone (DABP), or 3,3′-diaminodiphenylcarbinol (DADPC) and doped with Li2PdCl4 (LTP) or Pd[(CH3)2S]2Cl2 (PDS) were selected for a detailed x-ray photoelectron spectroscopic (XPS) study to determine the oxidation state of palladium and the relative distribution of this and other elements in these films, especially as they relate to electrical resistivity. XPS shows that Pd in the films is present as a mixture of zero and +2 valence states. Films that contain lithium as part of the dopant all show that metal is present as Li+ and Li2O, a fact that may have a bearing on film electrical properties. An Auger electron spectroscopic (AES) or XPS profiling was performed on two of the electrically conductive films. A film doped with PDS reveals a majority of palladium at the surface as Pd(0) and much smaller amounts in film bulk as a mixture of Pd(0) and Pd(II). Film behavior is similar to a metal-vapor deposited film. An LTP doped film, by contrast, exhibits a homogeneous composition with a mixture of Pd(0) and Pd(II). These studies support others that use chemical etching on the film surfaces. Scanning electron microscopy (SEM) has been used to provide surface evaluations. 相似文献
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Hydroxycarbonyls arising from OH-initiated reactions of isoprene have been quantified by the technique of a flow reactor coupled to proton-transfer reaction mass spectrometry (PTR-MS) detection. The yields of C5- and C4-hydroxycarbonyls are (19.3 +/- 6.1)% and (3.3 +/- 1.6)%, respectively, measured at a flow tube pressure of about 100 Torr and at a temperature of 298 +/- 2 K. A yield of (8.4 +/- 2.4)% is obtained for the unsaturated carbonyl C5H8O, confirming that internal OH addition represents the minor channel in the initial OH-isoprene reaction. The results show that those carbonyl compounds account for the most previously unquantified carbon, enabling the isoprene carbon closure. The study also reveals novel aspects of the delta-hydroxyalkoxy radical degradation mechanism, which is essential for modeling tropospheric O3 formation. In addition, this work demonstrates the application of PTR-MS for quantification of products of hydrocarbon reactions, which should have profound impacts on elucidation of the chemistry of atmospheric anthropogenic and biogenic hydrocarbons. 相似文献
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Paul Fortner 《Monatshefte für Chemie / Chemical Monthly》1893,14(1):146-164
Ohne Zusammenfassung 相似文献
10.
Dr. Max Fortner 《Monatshefte für Chemie / Chemical Monthly》1904,25(5):443-452
Ohne ZusammenfassungIch habe in meiner frÜheren Abhandlung Über das Benzoylfluoren die Zählung irrtÜmlicherweise mit dem der Methylengruppe benachbarten Kohlenstoffatom begonnen. Der Irrtum kam dadurch zustande, da\ Beilstein die von Gräbe aus Diphensäure dargestellte, nach der neuen Nomenklatur als Fluorenoncarbonsäure (4) zu bezeichnende Säure mit der Ziffer (5) versieht.Mit dem Studium dieser Frage bin ich gegenwärtig beschäftigt, weshalb ich das Ersuchen stelle, mir fÜr die nächste Zeit das bezÜgliche Arbeitsgebiet zu Überlassen. 相似文献