PREPARATION OF O2XEF2-X(OTEF5)X, OXEF4-Y(OTEF5)Y, AND XEF4-Y(OTEF5)Y (X = 0-2, Y = 0-4) AND STUDY BY XE-129 AND F-19 NMR AND RAMAN-SPECTROSCOPY - THE OXYGEN PRIMARY ISOTOPIC EFFECT IN THE XE-129 NMR-SPECTRA OF XEO2F2 AND XEOF4

被引：49

作者：

SCHUMACHER, GA ^{[1
]}

SCHROBILGEN, GJ ^{[1
]}

机构：

[1] MCMASTER UNIV,DEPT CHEM,HAMILTON L8S 4M1,ONTARIO,CANADA

来源：

INORGANIC CHEMISTRY | 1984年 / 23卷 / 19期

关键词：

D O I：

10.1021/ic00187a005

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

引用

页码：2923 / 2929

页数：7

共 8 条

[1] FXXE(OTEF5)3-X+, O=XEFX(OTEF5)3-X+ (X = 0-2), AND O2XEOTEF5+ CATIONS - THEIR PREPARATION AND CHARACTERIZATION IN SOLUTION BY XE-129 AND F-19 NMR-SPECTROSCOPY
SYVRET, RG
MITCHELL, KM
SANDERS, JCP
SCHROBILGEN, GJ
INORGANIC CHEMISTRY, 1992, 31 (16) : 3381 - 3385
[2] THE TE(OTEF5)(5) AND FTE(OTEF5)(4)(-) ANIONS - SYNTHESIS, X-RAY STRUCTURE DETERMINATIONS, AND RAMAN-SPECTRA OF TE(OTEF5)(4)(-) AND N(CH3)(4)TE-+(OTEF5)(5)- AND SOLUTION CHARACTERIZATION OF THE FTE(OTEF5)(4)(-) AND TE(OTEF5)(5)(-) ANIONS BY F-19 AND TE-125 NMR-SPECTROSCOPY
MERCIER, HPA
SANDERS, JCP
SCHROBILGEN, GJ
INORGANIC CHEMISTRY, 1995, 34 (21) : 5261 - 5273
[3] FXEOIOF4 AND XE(OIOF4)2 - PREPARATION AND STUDY BY X-129 AND F-19 NMR-SPECTROSCOPY AND RAMAN-SPECTROSCOPY AND NMR CHARACTERIZATION OF LXEOIOF4 (L = -OTEF5, -OSO2F)
SYVRET, RG
SCHROBILGEN, GJ
INORGANIC CHEMISTRY, 1989, 28 (08) : 1564 - 1573
[4] Synthesis and characterization by F-19 and Te-125 NMR and Raman spectroscopy of cis-ReO2(OTeF5)(3) and cis-ReO2(OTeF5)(4)(-) and X-ray crystal structure of [N(CH3)(4)(+)][cis-ReO2(OTeF5)(4)(-)]
Casteel, WJ
MacLeod, DM
Mercier, HPA
Schrobilgen, GJ
INORGANIC CHEMISTRY, 1996, 35 (25) : 7279 - 7288
[5] PREPARATION OF THE XEOTEF5+, FXEFXEOTEF5+, XEF2.BROF2+, AND XEOSO2F+ CATIONS AND THEIR STUDY BY XE-129,TE-125, AND F-19 PULSE FOURIER-TRANSFORM NMR AND RAMAN-SPECTROSCOPY
KELLER, N
SCHROBILGEN, GJ
INORGANIC CHEMISTRY, 1981, 20 (07) : 2118 - 2129
[6] Infrared and NMR spectra of arylsulphonamides, 4-X-C6H4SO2NH2 and i-X, j-YC6H3SO2NH2 (X = H; CH3; C2H5; F; Cl; Br; I or NO2 and i-X, j-Y = 2,3-(CH3)2; 2,4-(CH3)2; 2,5(CH3)2; 2-CH3, 4-Cl; 2-CH3, 5-Cl; 3-CH3, 4-Cl; 2,4-Cl2 or 3,4-Cl2)
Gowda, BT
Jyothi, K
D'Souza, JD
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION A-A JOURNAL OF PHYSICAL SCIENCES, 2002, 57 (12): : 967 - 973
[7] Infrared, 1H and 13C NMR spectra of N,N-dichloroarylsulphonamides, 4-X-C6H4SO2NCl2 (X = H, CH3, C2H5, F, Cl or Br) and i-X, j-YC6H3SO2 NCl2 (i-X,j-Y=2,3-(CH3)2, 2,4-(CH3)2, 2,5-(CH3)2, 2-CH3, 4-Cl, 2-CH3, 5-Cl, 3-CH3, 4-Cl, 2,4-Cl2 or 3,4-Cl2)
Gowda, BT
Jyothi, K
Damodara, N
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION A-A JOURNAL OF PHYSICAL SCIENCES, 2003, 58 (9-10): : 563 - 568
[8] Spectroscopic studies with N-chloroarylsulphonamides:: IR and 1H, 13C and 23Na NMR spectra of sodium salts of N-chloro-mono- and Di-substituted-benzenesulphonamides, 4-X-C6H4SO2NaNCl (X = H; CH3; C2H5; F; Cl; Br; I or NO2) and i-X,j-YC6H3SO2NaNCl (i-X,j-Y = 2,3-(CH3)2; 2,4-(CH3)2; 2,5-(CH3)2; 2-CH3,4-Cl; 2-CH3,5-Cl; 3-CH3,4-Cl; 2,4-Cl2 or 3,4-Cl2)
Gowda, BT
D'Souza, JD
Kumar, BHA
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION A-A JOURNAL OF PHYSICAL SCIENCES, 2003, 58 (01): : 51 - 56

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