全文获取类型
收费全文 | 90篇 |
免费 | 0篇 |
专业分类
化学 | 74篇 |
数学 | 5篇 |
物理学 | 11篇 |
出版年
2023年 | 1篇 |
2014年 | 1篇 |
2013年 | 3篇 |
2012年 | 1篇 |
2011年 | 1篇 |
2009年 | 2篇 |
2008年 | 2篇 |
2007年 | 1篇 |
2006年 | 3篇 |
2005年 | 1篇 |
2004年 | 2篇 |
2001年 | 3篇 |
1996年 | 2篇 |
1993年 | 2篇 |
1991年 | 3篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1987年 | 3篇 |
1986年 | 2篇 |
1985年 | 2篇 |
1984年 | 3篇 |
1983年 | 1篇 |
1982年 | 3篇 |
1981年 | 4篇 |
1980年 | 4篇 |
1979年 | 5篇 |
1978年 | 3篇 |
1977年 | 2篇 |
1976年 | 3篇 |
1975年 | 5篇 |
1974年 | 4篇 |
1973年 | 4篇 |
1972年 | 2篇 |
1971年 | 1篇 |
1970年 | 1篇 |
1968年 | 1篇 |
1966年 | 1篇 |
1965年 | 2篇 |
1963年 | 1篇 |
1960年 | 2篇 |
排序方式: 共有90条查询结果,搜索用时 31 毫秒
81.
Reactions of [(eta(6)-arene)RuCl(2)](2) 1 (arene = p-cymene (a), 1,2,3,4-Me(4)C(6)H(2) (b), 1,2,3-Me(3)C(6)H(2) (c)) with tris(2,6-dimethoxyphenyl)phosphine (TDMPP) led to loss of two molecules of CH(3)Cl to give (eta(6)-arene)Ru[{2-O-C(6)H(3)-6-OMe}(2){C(6)H(3)(OMe)(2)-2,6}], 2a-c, which contains a trihapto ligand (eta(3)-P,O,O) derived from TDMPP, whereas the 1,3,5-Me(3)C(6)H(3) (1d), 1,2,3,5-Me(4)C(6)H(2) (1e), and C(6)Me(6) (1f) complexes did not react with TDMPP. The structures of 2a and 2b were confirmed by X-ray analyses: for 2a, a = 11.691(2) ?, b = 15.228(2) ?, c = 10.320(1) ?, alpha = 95.93(1) degrees, beta = 113.783(9) degrees, gamma = 83.86(1) degrees, triclinic, P&onemacr;, Z = 2, R = 0.051; for 2b, a = 17.79(2) ?, b = 15.43(1) ?, c = 20.93(1) ?, beta = 91.25(8) degrees, monoclinic, P2(1)/n, Z = 8, R = 0.056. Bis(2,6-dimethoxyphenyl)phenylphosphine (BDMPP) reacted with 1a, 1b, and 1d at room temperature to give (eta(6)-arene)RuCl[PPh(2-O-C(6)H(3)-6-OMe){C(6)H(3)(OMe)(2)-2,6}], 3a,b,d, which contains a dihapto (eta(2)-P,O) ligand derived from BDMPP by an X-ray analysis of 3a: a = 12.33(1) ?, b = 14.246(8) ?, c = 11.236(9) ?, alpha = 91.47(8) degrees, beta = 117.28(6) degrees, gamma = 111.70(6) degrees, triclinic, P&onemacr;, Z = 2, R = 0.040. A similar reaction with 1f recovered the starting materials, but that in refluxing MeCN produced [(eta(6)-C(6)Me(6))Ru[PPh(2-O-C(6)H(3)-6-OMe}(2)], 4f, containing a trihapto (eta(3)-P,O,O) ligand derived from BDMPP. Complex 1d reacted with BDMPP at reflux in MeCN/CH(2)Cl(2) and resulted in a loss of an arene ring to give a five-coordinate complex, Ru[eta(2)-P,O-PPh(2-O-C(6)H(3)-6-OMe){C(6)H(3)(OMe)(2)-2,6}](2)(MeCN), 5. Treatment of (2,6-dimethoxyphenyl)diphenylphosphine (MDMPP) with 1f gave (eta(6)-C(6)Me(6))RuCl[eta(2)-P,O-PPh(2)(2-O-C(6)H(3)-6-OMe)],6f, and that with 1b gave (eta(6)-1,2,3,4-Me(4)C(6)H(2))RuCl[eta(2)-P,O-PPh(2)(2-O-C(6)H(3)-6-OMe}], 6b, and (eta(6)-1,2,3,4-Me(4)C(6)H(2))RuCl(2)[eta(1)-P-PPh(2){C(6)H(3)(OMe)(2)-2,6}],7b. The phosphine ligand of 6b acted as a bidentate ligand derived from MDMPP: a = 8.074(4) ?, b = 16.816(3) ?, c = 18.916(4) ?, beta = 94.05(3) degrees, monoclinic, P2(1)/n, Z = 4, R = 0.051. Transformation of 7b to 6b readily occurred accompanying an elimination of MeCl. Reaction of 1a with MDMPP eliminated an arene ring to give the octahedral compound RuCl(2)[eta(2)-P,OMe-PPh(2){C(6)H(3)(MeO)(2)-2,6}](2), 8. An X-ray analysis of 8 showed that two MDMPP ligands were in a cis-position: a = 10.596(14) ?, b = 27.586(12) ?, c = 13.036(8) ?, beta = 108.17(7) degrees, monoclinic, P2(1)/n, Z = 4, R = 0.035. 相似文献
82.
83.
Rokuro Muki Eli Sternberg 《Zeitschrift für Angewandte Mathematik und Physik (ZAMP)》1965,16(5):611-648
Zusammenfassung Es werden im Rahmen einer linearisierten Theorie, welche Spannungsmomente berücksichtigt, singuläre Spannungskonzentrationen untersucht. Zu diesem Zweck wird mit Hilfe der exponentiellen Fouriertransformation für das Problem der Halbebene unter verteilter Oberflächenbelastung im ebenen Verschiebungszustand eine exakte Lösung aufgestellt. Diese Lösung wird anschliessend zum Studium des singulären Spannungsfeldes benützt, welches sich unter konzentrierter Normal-oder Tangentiallast sowie unter unstetiger Schubbelastung einstellt; sie wird auch zur Ermittlung der Spannungskonzentration benützt, welche von einem flachen Stempel herrührt. In jedem Falle werden die erhaltenen Singularitäten im einzelnen studiert und mit den entsprechenden Singularitäten der klassischen Elastizitätstheorie verglichen.
This paper was prepared under Contral Nonr-220 (58) with the Office of Naval Research in Washington, D. C.
The work underlying this paper was carried out in part while the second author was a Guggenheim Fellow at Keio University, where he held a Visiting Professorship. 相似文献
This paper was prepared under Contral Nonr-220 (58) with the Office of Naval Research in Washington, D. C.
The work underlying this paper was carried out in part while the second author was a Guggenheim Fellow at Keio University, where he held a Visiting Professorship. 相似文献
84.
Hirobumi Ushijima Susumu Sudoh Masatsugu Kajitani Kunio Shimizu Takeo Akiyama Akira Sugimori 《应用有机金属化学》1991,5(4):221-228
Four novel cobalt(III) complexes with a cyclopentadienyl or pentamethylcyclopentadienyl ring and dmit or dmio ligands were synthesized, and their electrochemical behaviour was investigated. All these complexes exhibited three one-electron transfer steps: one reduction and two oxidation steps. In addition, a novel organosulphur compound was afforded by electrochemical oxidation of dmit cobalt complex. Thus, these complexes may have considerable synthetic potential as precursors for electron reservoirs and organosulphur compounds. 相似文献
85.
Hiroshi Hamaguchi Rokuro Kuroda Ryuitiro Sugisita Naoki Onuma Tsuneo Shimizu 《Analytica chimica acta》1963
A spectrophotometric study of the scandium-quercetin complex is described; μg amounts of scandium can be determined with quercetin at 43.5 mμ and pH 4.4. A 1:1 complex is formed. The apparent instability constant of the complex was estimated as 2.7·10-7 by a spectrophotometric method. An ion-exchange method for separating scandium from several interfering ions is described. 相似文献
86.
Junzo Nokami Kotaro Nishiuchi Shoji Wakabayashi Rokuro Okawara 《Tetrahedron letters》1980,21(46):4455-4456
2,4-Dienoate was prepared by pyrolysis of 2-(phenylsulfinyl)enoate. N-Isobutyl-E,E-2,4-decadieneamide (pellitorine) was synthesized from decanoic acid in a satisfactory yield. 相似文献
87.
Summary A flow-injection spectrophotometric method has been developed for the rapid, continuous determination of aluminium in copper-base alloys. The system consists of the masking of copper, zinc, iron, etc. with a combined use of thiourea, ascorbic acid and EDTA and the measurement of light absorption of aluminium-Xylenol Orange complex at 506 nm. With appropriate standardization satisfactory results are obtained in spite of sluggish reaction of aluminium and Xylenol Orange. The system allows the analysis of solutions of copper-base alloys for aluminium to be conducted at a rate of 50 determinations per hour without any carryover. The results obtained for standard brasses and aluminium bronze (Al 1.43–10.2%) agreed well with the certified values. The precision (rsd) ranges are 0.2–0.3%.
Kontinuierliches Schnellverfahren zur Bestimmung von Aluminium in Kupferlegierungen mit Hilfe der Flow-Injection-Spektralphotometrie
Zusammenfassung Bei dem empfohlenen Verfahren werden Cu, Zn, Fe und andere Störelemente mit Hilfe von Thioharnstoff, Ascorbinsäure und EDTA maskiert und der Al-Xylenolorange-Komplex bei 506 nm gemessen. Mit Hilfe eines geeigneten Eichverfahrens werden trotz der trägen Reaktion von Al mit Xylenolorange zufriedenstellende Werte erhalten. 50 Bestimmungen können innerhalb von 1 h ohne jedes Verschleppen durchgeführt werden. Bei der Analyse von Messing und Al-Bronze (1,43–10,2% Al) wurde gute Übereinstimmung mit zertifizierten Werten erzielt. Die Standardabweichungen lagen im Bereich von 0,2–0,3%.相似文献
88.
A systematic study is presented on the adsorption behavior of some 20 metals on a weakly basic condensed phenol resin, Amberlite CG-4B, in sulfuric acid media. The distribution coefficients were determined over a sulfuric acid concentration range of 0.005 M to 2 M. The metals adsorbed are similar to those which exhibit strong adsorption on a strongly basic resin, but the magnitudes of the distribution coefficients and the adsorption sequences differ considerably between the two types of the resin. Several two- and three-component separations of analytical interest are possible. A new method for the separation of titanium(IV) is described; this is based on its high adsorption on CG-4B from sulfuric acid media containing hydrogen peroxide. 相似文献
89.
Summary A dry-column Chromatographic technique has been applied to the separation of uranium from complicated matrices. It has been demonstrated that operating parameters of thin-layer chromatography on silanized silica gel in isopropyl ether-tetrahydrofuran-nitric acid (65203) can be transferred to this technique. Chromatograms are thus easily developed on dry packed column with the solvent system of the type used in the TLC. Uranium is eluted off the column and determined with Arsenazo III spectrophotometrically. The technique is successfully applied to the determination of uranium in monazite and phosphate rock samples with good precision and accuracy.
Trockensäulenchromatographie des Urans. Anwendung zur chemischen Analyse von Monazit und Phosphorit
Zusammenfassung Zur Abtrennung des Urans aus komplizierten Matrices wurde die Trockensäulenchromatographie verwendet. Wie gezeigt werden konnte, lassen sich die Bedingungen der Dünnschichtchromatographie (DSC) auf silanisiertem Silikagel mit Isopropylether-Tetrahydrofuran-Salpetersäure (65203) auf das genannte Verfahren übertragen. Chromatogramme sind daher auf trocken geschichteten Säulen mit Lösungsmittelsystemen der DSC herstellbar. Uran wird eluiert und mit Arsenazo III spektrophotometrisch bestimmt. Das Verfahren wurde zur Uranbestimmung in Monazit und Phosphorit erfolgreich angewendet.相似文献
90.
Keisuke Shigenobu Taku Sudoh Junichi Murai Kaoru Dokko Masayoshi Watanabe Kazuhide Ueno 《Chemical record (New York, N.Y.)》2023,23(8):e202200301
Highly concentrated electrolytes (HCEs) have a similarity to ionic liquids (ILs) in high ionic nature, and indeed some of HECs are found to behave like an IL. HCEs have attracted considerable attention as prospective candidates for electrolyte materials in future lithium secondary batteries owing to their favorable properties both in the bulk and at the electrochemical interface. In this study, we highlight the effects of the solvent, counter anion, and diluent of HCEs on the Li+ ion coordination structure and transport properties (e. g., ionic conductivity and apparent Li+ ion transference number measured under anion-blocking conditions, ). Our studies on dynamic ion correlations unveiled the difference in the ion conduction mechanisms in HCEs and their intimate relevance to values. Our systematic analysis of the transport properties of HCEs also suggests the need for a compromise to simultaneously achieve high ionic conductivity and high values. 相似文献