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1. |
A study of sensitized photooxygenation of 3,4‐dihydro‐2H‐pyran |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 1-6
Cao Yi,
Chen Jian‐Xin,
Zhang Bao‐Wen,
Ming Yang‐Fu,
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摘要:
AbstractThe photooxygenation of 3,4‐dihydro‐2H‐pyran sensitized by cyanoanthracenes (9,10‐dicyanoanthracene and 9‐cyanoanthracene) in different solvents (CH3CN, CH3Cl2,C6H6and CCl4) has been studied in this paper. The products, product distribution as well as solvent isotope effect are the same as those in the reaction of singlet oxygen. Fluorescence quenching, exciplex formation and free energy change also reveal that electron transfer occurs between sensitizer‐excited singlet state and substrate and then singlet oxygen is formed subsequently as the reactive intermediate in
ISSN:0256-7660
DOI:10.1002/cjoc.19860040102
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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2. |
Estimation of the lattice heat capacity of rare‐earth compounds |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 7-19
Zhang Zhi‐Ying,
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摘要:
AbstractOn the basis of the experimental data reported in literature, the contributions of cation mass (m) and molar volume (V) to lattice heat capacity (C) were analyzed. The volumetric‐mass formula,Cx=(l —f)·C1+f·C2+Cm·(mx—mx′), was presented for estimating the heat capacities of rare‐earth compounds. In the formulaC1andC2represent the lattice heat capacities of two reference substances respectively,f=Vx—V1/V2—V1andCmrepresents the lattice heat capacity variation with the variation 1 g of cation mass. The equation relating theCmwith temperatures was derived as follows:Cm= 0.084e−0.0074T−0.27e−0.045T, andmxandmx′ (= (1 ‐f)m1+fm2) represent the practical and “assumed” cation masses of the subs
ISSN:0256-7660
DOI:10.1002/cjoc.19860040103
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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3. |
Electron transfer reactions between vinylmagnesium bromide and phenyl‐substituted methyl chlorides |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 20-28
Liu You‐Cheng,
Dang Hai‐Shan,
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摘要:
AbstractThe reaction of vinylmagnesium bromide (1) with trityl chloride (2) was investigated and the products were identified as triphenylmethane (3) (81 %), acetylene (4) (74%), trityl peroxide (6) (4%), and minute amounts of triphenylpropene (7) andp‐diphenylmethyltetraphenylmethane (8). The results indicate that 1 possesses reducing property. The reaction mixture showed an ESR spectrum identical with that for trityl radical and the CIDNP of enhanced absorption for4‐Hof l‐diphenylmethylene‐4‐trityl‐2,5‐cyclohexadiene (9). Trapping experiment with styrene decreased the amount of3but had no effect on the formation of4.The reducing property of 1 is discussed and one electron transfer mechanism for the reaction of1with2is proposed.S‐T0mixing between trityl and·MgBr occurred and the coupling of polarized trityl radical with another trityl radical resulted in the formation of polarized dimeric product. The different character between the reaction of1and2and that of1and diphenylmethyl chloride (10) may be rationalized by the different electron‐accepting abilities between2and10.The origin of CIDNP effect shown by the product tetraphenylethane (11) for the reaction of1with10is also explained according to K
ISSN:0256-7660
DOI:10.1002/cjoc.19860040104
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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4. |
The Mössbauer spectra and coordination structure of some dialkyltin (IV) derivatives |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 29-34
Wang Xu‐Kun,
Liu Xiang‐Yang,
Xiao Lai,
Wang Yung‐Tai,
Yian Qi‐Je,
Xia Yuan‐Fu,
Wang Shu‐Xin,
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摘要:
AbstractFive newbis(β‐carbomethoxyethyl)tin derivatives including R2Sn(acac)2(R = CH2OCOCH2CH2), R1Sn(dbm)2,R2SnO, R′2Sn(dbm)2[R′=CH2OCOCH(CH3)CH2] and R′SnO were synthesized. The structures of these compounds were compared with R2SnCl2,R′2SnCl2,(C2H17)2SnCl2,and (C2H17)2Sn(OCOC11H2)2.H NMR, IR and Mössbauer spectroscopic data showed that R′2Sn(dbm)2contains acisC‐Sn‐C unit, (C2H17)2Sn(OCOC11H23)3exists as a mixture of two isomers, while the other compounds have
ISSN:0256-7660
DOI:10.1002/cjoc.19860040105
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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5. |
Stereochemical effects in mass spectra—Studies on mass spectra of epimers of podophyllotoxin and its derivatives |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 35-41
Yao‐Zu Chen,
Hua Su‐Ming,
Chen Nen‐Yu,
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摘要:
AbstractMass spectra of thirteen epimers of podophyllotoxin and its derivatives have been examined. By means of high resolution mass spectrometry, metastable ion scanning and isotopelabeling techniques, the effects of configuration of C1‐OH and condensed lactone ring on the fragmentation pattern and the relative abundances of characteristic ions in the mass spectra of these compounds have been studied and rationalize
ISSN:0256-7660
DOI:10.1002/cjoc.19860040106
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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6. |
On the studies of the vibrational spectra of cluster [Mo2O2S2(S2)2]2‐ |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 42-47
Liang Ying‐Qiu,
Zhao Wen‐Yun,
Xu Wei‐Qing,
Zhang Zhi‐Gui,
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摘要:
AbstractIR and Raman spectra of [Mo2O2S2(S2)2]2‐were reported. The resonance Raman spectra and the depolarization ratios in CH3CN solution were measured. By using the data of crystal structure, the simplified normal coordinate calculation of the stretching vibrations for anion [Mo2O2S2(S2)2]2‐was performed. The results obtained are useful to assign the vibrational bands of some Mo‐Fe‐S c
ISSN:0256-7660
DOI:10.1002/cjoc.19860040107
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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7. |
Mass spectrometry of maytansinoids—A study on the fragmentation mechanism and identification of synthetic analogs of maytansine |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 48-54
Yu Qi‐Tao,
Zhi‐Heng Huang,
Zhou Yun‐Li,
Zhou Qi‐Ting,
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摘要:
AbstractNatural maytansinoids and their synthetic intermediates (1—9) were studied by means of mass spectrometry upon electron impact condition. The fragmentation pathway and spectra‐structural relationship of these compounds were proposed. Based on the fragmentation pattern, structures of the synthetic analogs were identif
ISSN:0256-7660
DOI:10.1002/cjoc.19860040108
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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8. |
Total synthesis of (±)‐fangchinoline |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 55-61
Deng Ding‐An,
Pan Bai‐Chaun,
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摘要:
Abstract(±)‐Fangchinoline was synthesized by condensation of (±)‐1‐(3‐bromo‐4‐methoxy‐benzyl)‐2‐methyl‐6‐methoxy‐7‐hydroxy‐8‐bromo‐1,2,3,4‐tetrahydroisoquinoline (2) and (±)‐1‐(4‐hydroxy‐benzyl)‐2‐methyl‐6‐methoxy‐7‐hydroxy‐1,2,3,4‐tetrahydroisoquinoline (3)
ISSN:0256-7660
DOI:10.1002/cjoc.19860040109
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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9. |
Studies on the chemical constituents ofEucalyptus robustaSm.: Isolation and identification of robustaol B and other constituents |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 62-67
Qin Guo‐Wei,
Xu Ren‐Sheng,
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摘要:
AbstractNine known compounds, 5‐hydroxy‐4′,7‐dimethoxy‐6,8‐dimethylflavone, 4′,5‐dihydroxy‐7‐methoxy‐6,8‐dimethylflavone, 3β‐hydroxy‐urs‐11‐ene‐28‐oic‐13(28)‐lactone, 3β‐acetoxy‐urs‐11‐ene‐28‐oic‐13(28)‐lactone, uvaol, β‐sitosterol, 7β‐O‐glucoside of 5,7‐dihydroxy‐2‐methylchromone, 1‐triacontanol and 1‐triacontanoic acid, and a new acylphloroglucinol named robustaol B 6 were isolated from the leaves ofEucalyptus robustaSm.6was shown to be 4,6‐dihydroxy‐2‐methoxy isobutyrophenone by spectral analyses and was confirmed by synthesis.6sh
ISSN:0256-7660
DOI:10.1002/cjoc.19860040110
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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10. |
Studies on sulfinatodehalogenation: IV. The sulfinatodebromination of primary perfluoroalkyl bromides and perfluoroalkylene α, ω‐dibromides |
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Acta Chimica Sinica English Edition,
Volume 4,
Issue 1,
1986,
Page 68-72
Huang Bing‐Nan,
Wang Bing‐Huang,
Wang Wei,
Huang Wei‐Yuan,
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摘要:
AbstractUsing PTC or cosolvent, both perfluoroalkyl bromides such as Br (CF2)2O(CF2)2SO2Na (1), Br(CF2)2OCF2CO2H (2), Cl(CF2)4Br (3), Cl(CF2Br (4),n‐C6F13Br (5),n‐C8F17Br (6), H(CF2)8Br (7), α, ω‐dibromides O(CF2CF2Br)2(8), Br(CF2)6Br (9) and Br(CF2)8Br (10) reacted readily with Na2S2O4in the presence of NaHCO3in aqueous solution to form the corresponding perfluoroalkane sulfinates NaO2S(CF2)2O(CF2)2SO2Na (11), NaO2S(CF2)2OCF2CO2Na (12), Cl(CF2)4SO2Na (13), Cl(CF2)2SO2Na (14),n‐C3F13SO2Na (15),n‐C8F17SO2Na (16), H(CF2)8SO2Na (17), α, ω‐disulfinates O(CF2CF2SO2Na)2(18), NaO2S(CF2)4SO2Na (19) and NaO2S(CF2)8SO2Na (20) in 66—97% yields. To this new and general reaction of perfluoroalkyl bromides, the name sulfinatodebromin
ISSN:0256-7660
DOI:10.1002/cjoc.19860040111
出版商:WILEY‐VCH Verlag
年代:1986
数据来源: WILEY
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