Journal of the Chemical Society, Part 5The Society., 1965 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Results 1-3 of 72
Page 6402
... Calc . for CH12S : C , 62 · 0 ; H , 10 · 4 ; S , 27.6 . Calc . for C , H , S : C , 67 · 7 ; H , 6 · 5 ; S , 25-75 % ) ; ( vii ) b . p . 23–31 ° / 0.1-0.2 mm . ( 2.777 g . ) ( Found : C , 66-2 ; H , 8.2 ; S , 25-8 ; thiol S , 22-9 , 23 · ...
... Calc . for CH12S : C , 62 · 0 ; H , 10 · 4 ; S , 27.6 . Calc . for C , H , S : C , 67 · 7 ; H , 6 · 5 ; S , 25-75 % ) ; ( vii ) b . p . 23–31 ° / 0.1-0.2 mm . ( 2.777 g . ) ( Found : C , 66-2 ; H , 8.2 ; S , 25-8 ; thiol S , 22-9 , 23 · ...
Page 6597
... calc . 625 574 366 Ge ( C ) calc . Frequency 434 ( cm . - 1 ) 419 329 ( C2 ) calc . 585 666 535 346 ( C2 ) calc . 403 453 419 303 obs . * 582 361 394 † obs . 417 320 362 † Ti ( C3 ) calc . 479 447 331 Sn ( C3 ) calc . 376 363 315 ( C2 ) ...
... calc . 625 574 366 Ge ( C ) calc . Frequency 434 ( cm . - 1 ) 419 329 ( C2 ) calc . 585 666 535 346 ( C2 ) calc . 403 453 419 303 obs . * 582 361 394 † obs . 417 320 362 † Ti ( C3 ) calc . 479 447 331 Sn ( C3 ) calc . 376 363 315 ( C2 ) ...
Page 6841
... Calc . for C , H2Cl , CrN ,: C , 19-1 ; H , 8-0 ; Cl ( total ) , 34.0 ; Cl ( ionic ) , 22.7 % ] . Chloropentakisethylaminechromium ( 111 ) chloride . Anhydrous chromic chloride ( 11.0 g . ) was added in small amounts to pure anhydrous ...
... Calc . for C , H2Cl , CrN ,: C , 19-1 ; H , 8-0 ; Cl ( total ) , 34.0 ; Cl ( ionic ) , 22.7 % ] . Chloropentakisethylaminechromium ( 111 ) chloride . Anhydrous chromic chloride ( 11.0 g . ) was added in small amounts to pure anhydrous ...
Contents
ptolyl | 5785 |
The crystal structure of dipotassium bistrimethylenedinitramine nickelate11 | 5801 |
Coordination compounds having carboxylic esters as ligands | 5826 |
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absorption acetic acid acetic anhydride acetone Amer amine anhydride aqueous atoms band benzene benzyl bond borazocine boron bromide Calc carbon carbon tetrachloride carbonyl CH₂ Chem chloride chloroform chromatography cm.¹ complex compounds concentration constants crystallised decomp derivatives dilute dissolved distilled eluted ester ethanol ether ethyl acetate evaporated extracted filtered filtrate fluoride Found fraction gave give H₂O heated under reflux hydrochloric acid hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum iodide isolated isomer ketone ligand light petroleum m. p. and mixed methyl mixed m. p. mixture mmoles mole molecule n.m.r. spectrum nitrogen obtained olefin optical oxazolone oxide peak perchlorate phenyl potassium prepared proton pyridine reaction requires residue ring room temperature salt showed sodium sodium hydroxide solid soluble solution solvent spectra structure sulphide sulphoxide sulphuric Table thionyl chloride vacuo values VIII yellow yield