Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
From inside the book
Results 1-3 of 3
Page 1315
... ة و -100 8 180 63 78 322 -353 166 -172 170 -33 -7 159 -113 10 269 230 232 104 -88 4 74 -55 144 III 4 136 210 12 . 49 77 238 83 -70 115 دو 164 160 73 209 -I -184 138 123 128 107 91 132 224 216 123 -ai -2 247 -238 20 I -107 141 223 -305 ...
... ة و -100 8 180 63 78 322 -353 166 -172 170 -33 -7 159 -113 10 269 230 232 104 -88 4 74 -55 144 III 4 136 210 12 . 49 77 238 83 -70 115 دو 164 160 73 209 -I -184 138 123 128 107 91 132 224 216 123 -ai -2 247 -238 20 I -107 141 223 -305 ...
Page 1867
... ة .رة 9 7.7 7.0 1.571 79.0 -3.107 3 30 20.1 18.7 3.143 3304 -3.560 14.0 1.578 • 49-5 -3.643 5308 9.8 0.000 37.4 -3.694 12.1 56.7 11.8 -3.Bas 1.733 39.7 96.3 91.9 5.3 3.143 35.9 0.001 43-4 19.7 8016 9.7 0.234 64.6-1.571 37.0 -1.500 ...
... ة .رة 9 7.7 7.0 1.571 79.0 -3.107 3 30 20.1 18.7 3.143 3304 -3.560 14.0 1.578 • 49-5 -3.643 5308 9.8 0.000 37.4 -3.694 12.1 56.7 11.8 -3.Bas 1.733 39.7 96.3 91.9 5.3 3.143 35.9 0.001 43-4 19.7 8016 9.7 0.234 64.6-1.571 37.0 -1.500 ...
Page 1868
... ة . -3.459 8 6 36 6 5 30.1 31-5 1.565 11.6 13.8 -3.500 O 10.6 10.9 3.542 • 23.j 3307 1.890 0.000 6 3401 35.9 0.210 14.2 23.2 11.3 13.0 2.054 308 1.571 22.9 21.6 3701 18.4 -0.387 2.916 11.9 1.708 3 6.0 6.9 0.85C -3.014 -0.658 1 10.1 6.0 ...
... ة . -3.459 8 6 36 6 5 30.1 31-5 1.565 11.6 13.8 -3.500 O 10.6 10.9 3.542 • 23.j 3307 1.890 0.000 6 3401 35.9 0.210 14.2 23.2 11.3 13.0 2.054 308 1.571 22.9 21.6 3701 18.4 -0.387 2.916 11.9 1.708 3 6.0 6.9 0.85C -3.014 -0.658 1 10.1 6.0 ...
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 |
Copyright | |
118 other sections not shown
Other editions - View all
Common terms and phrases
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
Bibliographic information
| Title | Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
| Author | Chemical Society (Great Britain) |
| Contributor | Royal Society of Chemistry (Great Britain) |
| Published | 1969 |
| Original from | the University of Michigan |
| Digitized | 2 Jun 2011 |
| Export Citation | BiBTeX EndNote RefMan |