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21.
Roy Edward Bruns Paul Martin Kuznesof James Elton Moore 《Journal of Molecular Structure》1975,29(2):211-223
CNDO molecular orbital calculations have been performed to analyze donor—acceptor interactions between molecular chlorine and benzene, toluene, mesitylene and hexamethylbenzene and the, as yet, unreported chlorine—hexafluorobenzene and carbon disulfide—benzene pairs. The stabilization energy and the dipole moment and its derivative (?p/?RCICI) calculated for the benzene—chlorine complex are in good agreement with the estimated experimental values. The trends in the experimental stabilization energies and the Cl-Cl vibrational frequencies with increasing methyl substitution appear to be well reproduced by the calculations. The charge transferred from the benzene donor is polarized toward the outer chlorine atom or sulfur atom. For hexafluorobenzene-chlorine the direction of electronic charge polarization is reversed from that of the benzene and methylbenzene complexes. The calculated results are discussed within the framework of Muliiken's simplified resonance theory for complexes. 相似文献
22.
The synthesis of the novel 1,2-dihydroindolo [1,7-ab][1,5]benzodiazepine ring system 4 is described. Condensation of 2-fluoronitrobenzene with indoline provided the starting material for the synthesis, 1-(2-nitrophenyl)indoline (1a) in high yield. The nitro group was reduced catalytically and the resulting amino function was acylated to afford the heterocycle percursor amide 3. Refluxing this amide in phosphorus oxychloride brought about a Bischler-Napieralski type cyclodehydration to form the target 1,2-dihydroindolo[1,7-ab][1,5]benzodiazepine ring system. Dehydrogenation of the latter led to the fully aromatic indolo[1,7-ab][1,5]benzodiazepine structure 5, while reduction with sodium borohydride provided the 1,2,6,7-tetrahydroindolo[1,7-ab]-[1,5]benzodiazepine tetracycle 6. 相似文献
23.
D ← X resonance enhanced three-photon excitation spectrum of iodine was observed by a cw intracavity absorption technique. Vibrational quantum numbers of D ← X transitions are given for every major spectral feature. The corresponding one-photon enhancement from the B state is evident from the one-photon vibrational assignment. The spectroscopic constants for the D state are v00 = 40 998 cm?1 ω′0 = 113 cm?1 and ω′0χ′0 = 0.045 cm?. 相似文献
24.
A method of analysing steady-state fluorescence quenching in compartmentalized systems is proposed which allows the evaluation of partition and binding constants where both association processes occur simultaneosly. The number of binding sites is shown to be dependent on the nature of the quencher. 相似文献
25.
Lithio-1,3-diarylformamidines undergo reaction with the monomeric and dimeric carbonyl chlorides of manganese and rhenium, [M(CO)5Cl] and [M(CO)4Cl2] to yield respectively the carbamoyl-formamidino [M(CO)4-CON(R)CHNR] and the formamidino [M(CO)4RNCHNR] types of complex. The carbamoyl complexes undergo decarbonylation to produce the formamidino complexes in low yield. 相似文献
26.
Bruce M. Howard William Fenical Edward V. Arnold Jon Clardy 《Tetrahedron letters》1979,20(31):2841-2844
The structure of a unique bromine-containing ketal, obtusin (), has been determined by spectral and X-ray crystallographic techniques. Obtusin is a natural component of the Mediteranean red alga . 相似文献
27.
The reaction of sodium hydride or potassium t-butoxide with methyl epoxycitronellate (1) in dimethylformamide affords a mixture of cis,cis-puleganolide (2) and cis,trans-puleganolide (3) in high yield. When the cyclization is conducted at 110°, the isomeric 2-isopropenyl-5-methylcyclopentanecarboxylic acids (8a–d) become the major products. It is demonstrated that γ-lactones undergo alkoxide-induced elimination to afford γ,δ-unsaturated acids. 相似文献
28.
Pre-resonance Raman spectra have been obtained for TCNQ and LiTCNQ in acetonitrile solution using an Ar+—Kr+ laser and a tunable rhodamine 6G dye laser. Using the theory of Albrecht and Hutley, we have calculated frequency factors for the intensity variations for several symmetric vibrational modes of each molecule. The observed spectra for TCNQ and LiTCNQ with violet, blue, and green excitation give evidence for B-type resonance enhancement due to vibronic mixing between at least two violet and ultraviolet transitions. The Raman spectra for LiTCNQ with yellow, orange, and red excitation show A-type enhancement due to a single electronic excitation in the near infrared. 相似文献
29.
Condensation of bis-(2-chloroethyl)phosphoramidic dichloride with 3′-amino-3′-deoxy-N,N-dimethyladenosine afforded the 2′,3′-cyclicphosphorodiamidate (III). By an improved synthesis, methyl 3-amino-3-deoxy-β-D-ribofuranoside was obtained as a model compound for conversion to the analogous 2,3-cyclicphosphorodiamidate (XII). Existence of the latter as two diastereomers due to phosphorus asymmetry was shown by nmr analysis, using comparison with the 5-(O-p-nitrobenzoate) (XIII) as a basis for assignments. 相似文献
30.
A three-step synthesis of bispidine ( 1 ) is described. Mannich condensation of N-benzyl-4-piperidone, formaldehyde, and benzylamine afforded N,N′-dibenzylbispidinone ( 5 ), which was reduced under modified Wolff-Kishner conditions to yield N,N′ -dibenzylbispidine ( 6 ). Catalytic debenzylation of this compound gave 1 . 相似文献