排序方式: 共有57条查询结果,搜索用时 15 毫秒
1.
G. Balducci L. Bencivenni G. De Rosa R. Gigli B. Martine S.Nunziante Cesaro 《Journal of Molecular Structure》1980
The infrared and Raman spectra of some cyclopentadienyl compounds of the transition metals, namely Ti(C5H5)Cl3 and M(C5H5)2Cl2 (M = Ti, Zr and Hf), are reported and discussed. The infrared spectra of the gaseous species isolated in argon matrices at 10 K provide structural information about the single molecules. Particular attention has been paid to the low-frequency region in order to achieve more reliable assignments for the internal-rotation modes. The structural data and the fundamental frequencies derived from the spectra are employed in a calculation of the thermodynamic functions for these compounds in the ideal gas state. 相似文献
2.
Benati L Bencivenni G Leardini R Minozzi M Nanni D Scialpi R Spagnolo P Zanardi G 《The Journal of organic chemistry》2005,70(8):3046-3053
Thermal reaction of various alpha-azido esters with Bu(3)SnH in refluxing benzene results in smooth production of 3-(tributylstannyl)-1-triazene adducts affording cyclized 1,2,3-triazol-4-ones in preference to reduced amines and thence provides a new useful method for the preparation of these triazole derivatives. In the presence of AIBN the occurrence of triazene products still remains important or even exclusive and, consequently, generation of the expected stannylaminyl radicals is seriously limited. With 2-azidomalonates and alpha-azido-beta-keto esters stannyltriazenes can similarly occur in the absence of the radical initiator, but in the latter cases the ensuing triazenes undergo preferential cyclization onto the ketone moiety to give reactive hydroxytriazolines. Contrary to alpha-azido esters, in the presence of AIBN alpha-azido-beta-keto esters as well as azidomalonates give rise only to the usual stannylaminyl radicals. A possible explanation for the different behavior of the mono- and dicarbonyl azides in the presence of AIBN is put forward. 相似文献
3.
The molecular structure of gaseous CsReO4 has been studied by matrix isolation IR spectroscopy. The 18O substitution experiments indicate a bidentate structure of C2v symmetry in which the perrhenate anion is slightly distorted from the tetrahedral geometry. 相似文献
4.
The vapour pressures of cytosine and thymine were measured using the torsion-effusion technique. The sublimation processes of cytosine and thymine were investigated over the temperature ranges 480–553 K and 420–503 K, respectively. The following pressure—temperature equations were derived by least-squares treatment of the vapour pressure data The standard sublimation enthalpies were obtained by second-and third-law treatment of the experimental data and the values ΔH0298 = 167 ± 10 kJ mole?1 and ΔH0298 = 138 ± 10 kJ mole?1 were derived for cytosine and thymine, respectively. IR and Raman spectra were recorded in the gas phase in order to evaluate the thermodynamic functions of gaseous cytosine and thymine. 相似文献
5.
The thermal functions S0T, -(G0T-H0O)/T and (H0T-H0O) have been calculated from structural and spectroscopic data for the gaseous organometallics C5H5BeX (X = Cl, Br and BH4), C5H5MX3 (M = Ti and Ge; X = Cl, Br and I) and CH3TiX3 (X = Cl, Br and I). The rotational barriers of the C5H5 and CH3 groups have been evaluated and discussed. 相似文献
6.
Marco Bellagamba Luigi Bencivenni Lorenzo Gontrani Leonardo Guidoni Claudia Sadun 《Structural chemistry》2013,24(3):933-943
In this work, we report a multitechnique (energy-dispersive X-ray diffraction, computational methods, and FTIR spectroscopy) study of the tautomeric equilibrium of 1,2,3-triazole, one of the few small nitrogen-containing eterocycles liquid at room temperature. The T-2H form (C 2v symmetry) is found to be strongly favored in gas and solid phases, whereas the neat liquid gives diffraction patterns that can be interpreted satisfactorily with the structure functions calculated from some molecular dynamics results for both T-2H and T-1H tautomers, although the T-2H form gives a slightly better agreement. 相似文献
7.
8.
A. BallaG. Bencivenni M. CapodiferroS. Cerioni P. CiambroneE. De Lucia G. De RobertisA. Di Domenico D. Domenici J. DongG. Felici M. GattaM. Jacewicz N. LacalamitaS. Lauciani R. LiuzziF. Loddo M. MongelliM. Morello V. PateraA. Pelosi M. PistilliL. Quintieri A. RanieriM. Schioppa E. TshadadzeV. Valentino 《Nuclear Physics B - Proceedings Supplements》2011,215(1):76-78
9.
Francesco De Vincentiis Giorgio Bencivenni Dr. Fabio Pesciaioli Andrea Mazzanti Dr. Giuseppe Bartoli Prof. Patrizia Galzerano Dr. Paolo Melchiorre Prof. Dr. 《化学:亚洲杂志》2010,5(7):1652-1656
The first catalytic method for the asymmetric aziridination of cyclic enones is described. The presented organocatalytic strategy is based on the use of an easily available organocatalyst that is able to convert a wide range of cyclic enones into the desired aziridines with very high enantiomeric purity and good chemical yield. Such a method may very well open up new opportunities to stereoselectively prepare complex chiral molecules that possess an indane moiety, a framework that is found in a large number of bioactive and pharmaceutically important molecules 相似文献