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71.
While an unequal population of rapidly interconverting left- and right-handed conformers of a helical oligomer can be detected by circular dichroism, precise quantification of a conformer ratio has not previously been achieved. We demonstrate, using a set of labeled peptide analogues, that simple analysis of peak separation in their (13)C NMR spectra at slow and fast exchange allows an accurate value for the ratio of helical conformers to be obtained. The method reports the ratio of conformers at the site of the label and can therefore be used to investigate local variations in helical conformational control. 相似文献
72.
An indole-templated ring-closing metathesis has been used to create the central nine-membered ring of the cleavamine-type alkaloids. A subsequent intramolecular vinyl halide Heck reaction upon the resulting azacyclononene ring completes the assembly of the strained 1-azabicyclo[6.3.1]dodecane framework of the alkaloids. The usefulness of the approach is illustrated with the synthesis of (±)-cleavamine and (±)-dihydrocleavamine. 相似文献
73.
74.
Serrano I López MI Ferrer Í Poater A Parella T Fontrodona X Solà M Llobet A Rodríguez M Romero I 《Inorganic chemistry》2011,50(13):6044-6054
The synthesis of a family of new Ru complexes containing the facial tridentate ligand with general formula [Ru(II)(T)(D)(X)](n+) (T = trispyrazolylmethane (tpm); D = ((4S,4'S)-(-)-4,4',5,5'-tetrahydro-4,4'-bis(1-methylethyl)-2,2'-bioxazole) (iPr-box-C) or N-(1-hydroxy-3-methylbutan-(2S)-(-)-2-yl)-(4S)-(-)-4-isopropyl-4,5-dihydrooxazole-2-carbimidate (iPr-box-O); X = Cl, H(2)O) has been described. All complexes have been spectroscopically characterized in solution through (1)H NMR and UV-vis techniques, and the redox properties of complexes have also been studied by means of cyclic voltammetry (CV). Furthermore, the chloro complexes presented here have been characterized in the solid state through monocrystal X-ray diffraction analysis. The oxazolinic iPr-box-C ligand undergoes a Ru-assisted hydrolysis reaction generating the corresponding amidate anionic ligand iPr-box-O, that keeps coordinated to the Ru metal center and that produces a strong σ-donation effect over it. The reactivity of the Ru-OH(2) complexes described in this paper together with other similar ones, previously synthesized by us, has been tested with regard to the epoxidation of different olefins. Complexes [Ru(II)(R-box-C)(tpm)OH(2)](BF(4))(2), R = Bz, 3'c/iPr, 3c, show high stereoselectivity in the epoxidation of cis-β-methylstyrene, with the exclusive formation of the cis-epoxide. However, there is a significant difference in regioselectivity between the two catalysts in the epoxidation of 4-vinylcyclohexene; complex 3'c leads to the regioselective oxidation at the ring alkene position, whereas complex 3c leads to the oxidation at the terminal position. Computational calculations indicate only small energy differences between the two possible products of 4-vinylcyclohexene epoxidation, but the energy barriers for the interaction of the catalytic systems with the alkene groups of 4-vinylcyclohexene agree with the reactivity differences found for the two catalysts having isopropyl or benzyl as substituent of the oxazole ligand. Computed local Fukui functions help to explain the observed reactivity trends. 相似文献
75.
The concepts of conjugation and hyperconjugation play an important role to provide an explanation for several fundamental phenomena observed in organic chemistry. Because these effects cannot be directly measured experimentally, their assessment became a primary concern for chemists from the very beginning. In general, the stabilization produced by both phenomena has been studied by means of isodesmic reactions and energy based analysis such as the energy decomposition analysis. In recent years, electronic delocalization measures have been successfully applied to elucidate the nature of chemical bonding and the aromatic character of all kind of molecules. Because conjugation and hyperconjugation stabilizations are strongly linked to the concept of electron delocalization, this paper will give an account of both effects from the point of view of electronic delocalization measures calculated within the framework of the quantum theory of atoms in molecules. In particular, we focus our attention in the controversial case of the stabilization by conjugation in 1,3-butadiyne and 1,3-butadiene. Unexpectedly, theoretical calculations based on the scheme proposed by Kistiakowsky to quantify the extent of stabilization due to conjugation predicted that the conjugation of 1,3-butadiyne was zero. Subsequent energetic analyses contradicted this observation. These studies pointed out the presence of hyperconjugation stabilization in the hydrogenated product of 1,3-butadiyne and 1,3-butadiene that were used as reference systems in the Kistiakowsky's scheme. Consequently, the extra stabilization of 1-butyne due to hyperconjugation hides the stabilization by conjugation of 1,3-butadiyne. Our results based on electron delocalization measures confirm both the presence of conjugation in 1,3-butadiene and 1,3-butadiyne and hyperconjugation stabilization in their respective hydrogenated products, 1-butene and 1-butyne. 相似文献
76.
Roe C Moragas Solá T Sasraku-Neequaye L Hobbs H Churcher I MacPherson D Stockman RA 《Chemical communications (Cambridge, England)》2011,47(26):7491-7493
The synthetic utility of S-mesitylsulfinimines for the synthesis of chiral amines and aziridines was examined through their reactions with Grignard reagents, with the ylides derived from trimethylsulfonium iodide and S-allyl-tetrahydrothiophenium bromide and through an aza-Darzens manifold, affording convenient access to a diverse range of highly substituted chiral amines and aziridines in high yields and excellent stereoselectivities. 相似文献
77.
Imaz I Rubio-Martínez M An J Solé-Font I Rosi NL Maspoch D 《Chemical communications (Cambridge, England)》2011,47(26):7287-7302
Biomolecules are the building blocks of life. Nature has evolved countless biomolecules that show promise for bridging metal ions. These molecules have emerged as an excellent source of biocompatible building blocks that can be used to design Metal-Biomolecule Frameworks (MBioFs). This feature article highlights the advances in the synthesis of this class of MOFs. Special emphasis is provided on the crystal structures of these materials, their miniaturization to the submicron length scale, and their new potential storage, catalytic, and biomedical applications. 相似文献
78.
L. Escobar-Alarcón J. Pérez-Álvarez D. Solís-Casados Enrique Camps S. Romero J. Jiménez-Becerril 《Applied Physics A: Materials Science & Processing》2013,110(4):909-913
Co:TiO2 thin films were deposited using two interacting plasmas produced from different targets, TiO2 and cobalt. By keeping constant the laser ablation conditions on the TiO2 target and changing them on the Co target, it was possible to vary in a controlled way the Co content in the films. The cobalt plasma parameters, such as the ion kinetic energy and plasma density, were determined for each deposition condition in an attempt to correlate them with the material’s properties. The cobalt ion mean kinetic energy was varied from 36 to 789 eV, resulting in films with Co content from 1.2 up to 5.1 at.%, respectively, revealing that the cobalt content can be controlled by the Co+ kinetic energy. The study of the optical properties showed that the optical band gap decreased from 2.9 to 2.0 eV as the Co content increased. Raman spectroscopy was used to characterize the microstructure of the deposits, and the obtained results suggest the formation of two coexisting phases: TiO2 in its rutile phase and CoTiO3. It was found that as the Co+ energy increases, the CoTiO3 phase develops in a greater quantity. XPS measurements confirm the Raman spectroscopy results. 相似文献
79.
80.
Joseph A. Nuth Sol Glicker 《Journal of Quantitative Spectroscopy & Radiative Transfer》1982,28(3):223-231
Quantitative vacuum ultraviolet absorption spectra for HCN, C2N2, and CH3CN have been obtained over the wavelength range 60 nm ? λ ? 160 nm. Where comparison is possible, our measurements of the absorption coefficients for HCN and C2N2 are consistent with previous studies. Because of the superior resolution of this work (0.05 nm), vibrational assignments in the valence and Rydberg transitions of HCN have been extended while higher members of the Rydberg series in CH3CN have been identified. 相似文献