Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
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Page 1081
... gave a yellow band eluted with light petroleum , followed by [ ( π - C2H ̧ ) Fe ( CO ) 2 ] 2 ( 380 mg . , 21 % ) , eluted with benzene . The first product was recrystallised from light petroleum to give yellow crystals of p - MeC , F1 ...
... gave a yellow band eluted with light petroleum , followed by [ ( π - C2H ̧ ) Fe ( CO ) 2 ] 2 ( 380 mg . , 21 % ) , eluted with benzene . The first product was recrystallised from light petroleum to give yellow crystals of p - MeC , F1 ...
Page 1354
... gave type B behaviour after its first reduction at 401 ° ; it was then set aside in air at room temperature for a week before being reduced again at 195 ° . This catalyst , now designated Ni - P - 3b , gave type A behaviour . Further ...
... gave type B behaviour after its first reduction at 401 ° ; it was then set aside in air at room temperature for a week before being reduced again at 195 ° . This catalyst , now designated Ni - P - 3b , gave type A behaviour . Further ...
Page 2065
... gave pale yellow crystals which were washed with methylene chloride and ether to give bromodibromovinylbis ... gave trans - PtCl ( CC1 = CC12 ) ( PPh3 ) 2 ( 0-4 g . , 72 % ) . ( b ) With trichloroethylene . ( i ) As in ( a ) ( i ) ...
... gave pale yellow crystals which were washed with methylene chloride and ether to give bromodibromovinylbis ... gave trans - PtCl ( CC1 = CC12 ) ( PPh3 ) 2 ( 0-4 g . , 72 % ) . ( b ) With trichloroethylene . ( i ) As in ( a ) ( i ) ...
Contents
Dolcetti G See Peloso A 1506 | 1031 |
Structures of cyclic amides Part III Thio and selenolactams | 1033 |
Equilibria in solutions which contain a metal ion and an aminoacid | 1039 |
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¹H n.m.r. spectrum absorption acetaldehyde acetone acid adduct Amer anion aqueous atoms bands benzene bond bromine trifluoride calculated carbon catalyst cation Chem chemical Chemistry chloride cm.¹ co-ordination cobalt(II coefficients complexes compounds concentration configuration corresponding coupling constant crystals cyanide dehy gel dichloromethane dilute doublet electronic energy equation ethanol ether experimental Figure five-co-ordinate fluorine formation frequencies halide heat hydrogen hydrogen cyanide hydrolysis i.r. spectra Inorg iodide iodobenzene isomers k₁ kcal lactams ligand magnetic Mc./sec measured metal methyl mixture mmoles mole-¹ molecular molecule n.m.r. spectra nickel nickel(II nitric oxide nitrogen observed obtained octahedral orbital oxygen parameters phosphine phosphorus Phys plexes PMe,Ph potassium prepared present proton Raman reaction resonance room temperature sample scandium(III showed shown similar sodium solid solution solvent species structure sulphur Table thallium thio thiocyanate thiocyanogen thiolactams titration trans trimethylsilyl tris(trimethylsilyl values yellow