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41.
Günter Schmid 《Angewandte Chemie (International ed. in English)》1970,9(11):819-830
“True” metal-boron compounds have been known for about ten years. The bonding between the metal and boron atoms can vary widely in nature: Not only simple covalent bonds are encountered but also coordinate bonds and boron-metal multicenter bonds. Furthermore, π complexes of transition metals with boron-nitrogen systems and metal complexes containing boron(I) compounds as ligands have recently also been prepared. 相似文献
42.
A synthesis and stereochemistry confirmation of a constituent recently isolated from the whole plant Isodon excisus is reported. An enantioselective catalytic boron-mediated reduction of an α-bromoketone was utilized in the key synthetic transformation. The methodology described herein was also used for the synthesis of the natural product's enantiomer and several derivatives. In addition, the compounds were evaluated for inhibitory activity in a caspase induction assay. The natural product was found to be devoid of activity, but several derivatives had moderate inhibitory activity (EC50<1 μM). 相似文献
43.
非晶态NiP(B)/Al2O3催化一氧化碳,水和氧气合成过氧化氢 总被引:1,自引:0,他引:1
Hydrogenperoxideisagreenoxidantwithgreatpotentialformuchapplication .Thepresentproduc tionofhydrogen peroxiderequiressevereconditionsand generates pollutants .AlternativesynthesesarerequiredandthesynthesisofH2 O2 fromCO ,H2 OandO2 isverypromising .AsshowninEq(1) ,thesynthesisisthermodynamicallyfavored :CO +H2 O +O2 H2 O2 +CO2 (1)ΔG02 98=- 134kJ/mol ThereactionwasfirstreportedbyZudinetal[1]whousedpalladiumtriphenylphosphaneasacatalyst.Bianchietal[2 ] usedabiphasesystemforthesynthe … 相似文献
44.
45.
The paper presents a comparative analysis of the possibilities and characteristic features of the application of various polyhedral boron compounds, viz., the closo-decaborate anion [B10H10]2–, the closo-dodecaborate anion [B12H12]2–, the carba-closo-dodecaborate anion [CB11H12]–, carboranes C2B10H12, and the bis(dicarbollide) complexes [M(C2B9H11)2]– (M = Fe, Co, or Ni), in boron neutron capture therapy (BNCT) for cancer. The requirements on compounds used in BNCT are formulated and the advantages of the application of the closo-dodecaborate anion are considered. The data on the synthesis of various derivatives of the closo-dodecaborate anion, which either already found use in BNCT or are most promising in this field, are summarized. The possibilities of the application of agents derived from the closo-dodecaborate anion in medical diagnostics are discussed. 相似文献
46.
Soncini A Domene C Engelberts JJ Fowler PW Rassat A van Lenthe JH Havenith RW Jenneskens LW 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(4):1257-1266
Why are some (4n+2)π systems aromatic, and some not? The ipsocentric approach to the calculation of the current density induced in a molecule by an external magnetic field predicts a four‐electron diatropic (aromatic) ring current for (4n+2)π carbocycles and a two‐electron paratropic (antiaromatic) current for (4n)π carbocycles. With the inclusion of an electronegativity parameter, an ipsocentric frontier‐orbital model also predicts the transition from delocalised currents in carbocycles to nitrogen‐localised currents in alternating azabora‐heterocycles, which rationalises the differences in (magnetic) aromaticity between these isoelectronic π‐conjugated systems. Ab initio valence‐bond calculations confirm the localisation predicted by the naïve model, and coupled‐Hartree–Fock calculations give current‐density maps that exhibit the predicted delocalised‐to‐localised/carbocycle–heterocycle transition. 相似文献
47.
B. V. Bukvetskii E. V. Fedorenko A. G. Mirochnik V. E. Karasev 《Journal of Structural Chemistry》2007,48(6):1148-1151
The crystal structure of boron difluoride 3-phenylthiopentane-2,4-dionate was determined. The relationship between the structure and luminescent properties is traced in the series of boron difluoride acetyl acetonates (acetyl acetonate, phenylacetyl acetonate, and phenylthioacetyl acetonate). The presence of the π stacking interactions in boron difluoride phenylthioacetyl acetonate crystals leads to increased intensity and bathochromic shift of the fluorescence band. 相似文献
48.
B3LYP/6-31G* density functional theory calculations have been carried out on the structure and stability of ten B20N20 clusters. It was found that two new proposed isomers with two octagons, twelve hexagons, eight squares in Cab and C2 symmetry were more stable than the isomer with sixteen hexagons and six squares in C2 symmetry which was previously deemed to the most stable by 79.5 and 13.8 kJ/mol respectively. The isomer with two decagons in S10 symmetry is much higher in energy than the most stable structure in C4h symmetry by 637.2 kJ/mol. 相似文献
49.
Anatoliy Nechepurenko 《Journal of solid state chemistry》2004,177(2):616-618
The investigation of sintering conditions for magnesiothermic amorphous boron (MgmBn) powder is presented. The results of chemical and X-ray analyses of magnesiothermic boron (MgmBn) indicate that it consists of amorphous boron MgB12 and a lesser amount of β-rhombohedral boron. The MgmBn-sintering process is determined by the conditions of amorphous boron transformation into β-boron (crystallization), such as the process of decomposition of MgB12 followed by formation of the “new” centers of active elementary boron. As a result of the experimental investigations of this process the following three stages—thermal decompositions, crystallization and MgmBn sintering—were combined into one sintering process with the sintered bodies as a result of it. 相似文献
50.
Stíbr B Holub J Bakardjiev M Pavlík I Tok OL Císarová I Wrackmeyer B Herberhold M 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(10):2239-2244
The reaction of nido-[7,8,9-PC(2)B(8)H(11)] (1) with [[CpFe(CO)(2)](2)] (Cp=eta(5)-C(5)H(5) (-)) in benzene (reflux, 3 days) gave an eta(1)-bonded complex [7-Fp-(eta(1)-nido-7,8,9,-PC(2)B(8)H(10))] (2; Fp=CpFe(CO)(2); yield 38 %). A similar reaction at elevated temperatures (xylene, reflux 24 h) gave the isomeric complex [7-Fp-(eta(1)-nido-7,9,10-PC(2)B(8)H(10))] (3; yield 28 %) together with the fully sandwiched complexes [1-Cp-closo-1,2,4,5-FePC(2)B(8)H(10)] 4 a (yield 30%) and [1-Cp-closo-1,2,4,8-FePC(2)B(8)H(10)] 4 b (yield 5%). Compounds 2 and 3 are isolable intermediates along the full eta(5)-complexation pathway of the phosphadicarbaborane cage; their heating (xylene, reflux, 24 h) leads finally to the isolation of compounds 4 a (yields 46 and 52%, respectively) and 4 b (yields 4 and 5%, respectively). Moreover, compound 3 is isolated as a side product from the heating of 2 (yield 10%). The structure of compound 4 a was determined by an X-ray structural analysis and the constitution of all compounds is consistent with the results of mass spectrometry and IR spectroscopy. Multinuclear ((1)H, (11)B, (31)P, and (13)C), two-dimensional [(11)B-(11)B]-COSY, and (1)H[(11)B(selective)] magnetic resonance measurements led to complete assignments of all resonances and are in excellent agreement with the structures proposed. 相似文献