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991.
Four new triphenylgermylruthenium carbonyl compounds HRu(CO)4GePh3, 14; Ru(CO)4(GePh3)2, 15; Ru2(CO)8(GePh3)2, 16; and Ru3(CO)9(GePh3)3(μ-H)3, 17 were obtained from the reaction of Ru(CO)5 with Ph3GeH in hexane solvent at reflux, 68 °C. The major product 14 was formed by loss of CO from the Ru(CO)5 and an oxidative addition of the GeH bond of the Ph3GeH to the metal atom. This six coordinate complex contains one terminal hydrido ligand. Compound 15 is formed from 14 and contains two trans-positioned GePh3 ligands in the six coordinate complex. Compound 16 contains two Ru(CO)4(GePh3) fragments joined by an Ru–Ru single bond. Compound 17 contains a triangular cluster of three ruthenium atoms with three bridging hydrido ligands and one terminal GePh3 ligand on each metal atom. When heated to 125 °C, 14 was converted to the new triruthenium compound Ru3(CO)10(μ-GePh2)2, 18. Compound 18 consists of a triangular tri-ruthenium cluster with two GePh2 ligands bridging two different edges of the cluster and one bridging CO ligand. Ru3(CO)12 was found to react with Ph3GeH at 97 °C to yield three products: 15, and two new compounds Ru3(CO)9(μ-GePh2)3, 19 and Ru2(CO)6(μ-GePh2)2(GePh3)2, 20 were obtained. Compound 19 is similar to 18 having a triangular tri-ruthenium cluster but has three bridging GePh2 ligands, one on each Ru–Ru bond. Compound 20 contains only two ruthenium atoms joined by a single Ru–Ru bond that has two bridging GePh2 ligands and a terminal GePh3 ligand on each metal atom. All compounds were characterized by a combination of IR, 1H NMR, single-crystal X-ray diffraction analyses.
This report is dedicated to Professor Dieter Fenske on the occasion of his 65th birthday for his many pioneering contributions
to the chemistry of metal chalcogenide cluster complexes. 相似文献
992.
993.
Stable oxygen isotopic compositions of a coral colony ofPorites lutea obtained on a core allowed the reconstruction of a 56-a (1943–1998) proxy record of the sea surface temperatures. This coral δ18O data are from the east of Hainan Island water (22°20’N, 110°39’E), South China Sea. The relationship between δ18O in the skeletal aragonite carbonate and the sea surface temperature (SST) is SST = -5.36 δ18OPDB-3.51 (r = 0.73,n = 470), dδ18O/d(SST) = -0.187?/ °C; and the thermometer was set at monthly resolution. The 56-a (1943–1998) proxy record of the sea surface temperatures reflected the same change trend in the northern part of South China Sea as the air temperature change trend in China. 相似文献
994.
A solid state copper(II) ion sensor is reported based on the application of electropolymerized undoped (neutral) polycarbazole
(PCz) and polyindole (PIn) modified electrodes. The new sensor shows high selectivity to Cu2+ ions with a detection limit of 10–5 M. PCz and PIn are formed respectively by the anodic oxidation of 50 mM carbazole and 5 mM indole monomers in dichloromethane
containing 0.1 M tetrabutylammonium perchlorate on a platinum electrode using a single compartment cell. Potentiostatic polymerization
of both the monomers are carried out at 1.3 V and 1.0 V vs. Ag/AgCl, respectively. Perchlorate ions were electrochemically
removed from the polymer films by applying – 0.2 V vs. Ag/AgCl. Polymer-coated electrodes are incubated in 1 M KCl solution
for 8 h followed by incubation in distilled water for 2 h before using as a metal ion sensor. The undoped PCz and PIn electrodes
were found to be highly selective and sensitive for Cu2+ ions with little selectivity for Pb2+ and negligible response towards Ag+, Hg2+, Cu+, Ni2+, Co2+, Fe2+, Fe3+ or Zn2+. Potentiometric responses for Cu2+ ions are recorded for both the sensor electrodes together with a double-junction Ag/AgCl reference electrode. Calibration
curves for Cu2+ are reported for both ion sensors. The polymer-modified electrodes were found to be stable for several weeks.
Electronic Publication 相似文献
995.
In this paper, the use of an ion-pairing reagent to improve the separation selectivity of inorganic anions in CZE was demonstrated by the addition of tetramethylammonium hydroxide (TMAOH) to the electrolyte. The separation of inorganic anions (Cl(-), I(-), Br(-), NO(2)(-), NO(3)(-) and SCN(-)) was performed using co-electroosmotic flow (EOF) with direct UV detection at 185 nm. The parameters affecting the mobility of the tested anions and the EOF such as the electrolyte pH and concentration of TMAOH in the electrolyte were examined to optimise the separation conditions. In addition, sample-stacking techniques were investigated to improve detection sensitivity. Detection sensitivities were improved 5-13-fold using electrokinetic sample stacking. The detection limits ranged from 1-3 micro mol L(-1). Finally, the proposed method was used for the separation of anions in groundwaters. 相似文献
996.
[reaction: see text] Highly stereodivergent Woodward-Prevost reaction applied to iodoacetates derived from homochiral alpha-amino acids afforded enantiopure 3,4-cis- and 3,4-trans-pyrrolidinediol derivatives, with control over the protecting group, allowing for differential protection. 相似文献
997.
Inha Park J. W. Barlow D. R. Paul 《Journal of polymer science. Part A, Polymer chemistry》1991,29(9):1329-1338
Polystyrene chains with terminal anhydride groups were synthesized by direct chain transfer reaction between poly(styryl) lithium and trimellitic anhydride chloride (TMAC) and by the alkoxy-de-halogenation reaction between TMAC and hydroxy terminated polystyrene. Pyridine was used as a catalyst for these nucleophilic substitution reactions. For the direct reaction a poly(styryl) lithium with M?n ~ 1000 (a low MW was used for characterization purposes) was prepared in an argon purged reactor and then introduced into an excess of trimellitic anhydride chloride. Due to the nature of our reaction system, the molecular weight distributions obtained were broader than those possible using more stringent high vacuum techniques. Hydroxy terminated polystyrenes with M?n = 3,000 and 13,000 obtained elsewhere were used for the indirect addition of terminal anhydride groups. 1H-NMR spectroscopy, gel permeation chromatography (GPC), and FTIR spectroscopy were used to characterize the reaction products. A maximum yield of 61% for the direct functionalization route and 85% for the indirect functionalization route using hydroxyl terminated polystyrene were achieved. The higher yield of the indirect method seems to be the result of the relatively mild reactivity of the hydroxyl group. 相似文献
998.
Isothermal vapor–liquid equilibrium data determined by the static method at 303.15 K are reported for the binary systems propyl vinyl ether + 1-propanol, 1-propanol + 2,2,4-trimethylpentane and propyl vinyl ether + 2,2,4-trimethylpentane and also for the ternary system propyl vinyl ether + 1-propanol + 2,2,4-trimethyl-pentane. Additionally, new excess volume data are reported for the same systems at 298.15 K. The experimental binary and ternary vapor–liquid equilibrium data were correlated with different GE models and excess molar volume data were correlated with the Redlich–Kister equation for the binary systems and the Cibulka equation for the ternary system, respectively. 相似文献
999.
Shi-Xing Liu Ya-Qiu Lang Xue-Shen Liu Pei-Zhu Ding Yue-Ying Qi 《Journal of mathematical chemistry》2007,41(2):113-122
The classical dynamics of 1D H2+ in an intense field are discussed. The initial conditions are chosen at random in the field-free case, and then the Hamiltonian
canonical equations of H2+ system in the intense laser field are solved numerically by mean of the symplectic method under these initial conditions.
The probabilities of survival, dissociation, ionization, and Coulomb explosion of H2+ system in the intense laser field are obtained for different laser intensity based on the classical theory. 相似文献
1000.
William Doherty Peter Halley Les Edye David Rogers Francisco Cardona Yoosup Park Tim Woo 《先进技术聚合物》2007,18(8):673-678
Sugarcane fiber (i.e. bagasse) lignin has a larger fraction of aromatics unsubstitution in the ortho position than hardwood or softwood lignin and hence has the greater ability to be derivatized. Furthermore, organosolv lignin has a higher purity than sulfonated and kraft lignins. This work examines the purification of organosolv lignin derived from bagasse and the physico‐chemical properties of the lignin and lignin‐phenol formaldehyde (PF) resin coatings, and composites. The wetability tests have shown that lignin and lignin‐PF resin films are effective water barrier coatings, though the contact angles of lignin‐PF resin films were considerably less than the wax films. The overall mechanical properties (i.e. peak stress, peak strain and modulus) of the bagasse fiber composites were lower than the values obtained with the composites without the inclusion of bagasse fiber. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献