Quarterly Journal of the Chemical Society of London, Part 1, Pages 1033-2076 |
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Page 1642
... orbitals become more compact , a tendency that was first noted in a similar comparison for the 3d orbitals of sulphur.37 The trends of orbital exponents and energies in Table 2 for valence states are consistent with those in Table 1 for ...
... orbitals become more compact , a tendency that was first noted in a similar comparison for the 3d orbitals of sulphur.37 The trends of orbital exponents and energies in Table 2 for valence states are consistent with those in Table 1 for ...
Page 1643
... orbital and orbitals on the ligands , par- ticularly the bonding orbitals . Explicit account of these cases of non - orthogonality must increase the energy , but this should be greatest for the completely ionic structure and least for ...
... orbital and orbitals on the ligands , par- ticularly the bonding orbitals . Explicit account of these cases of non - orthogonality must increase the energy , but this should be greatest for the completely ionic structure and least for ...
Page 2003
... orbital ( solid line ) composed of hybrid boron orbitals ( broken lines ) show that this similarity arises from topological aspects of the problem ; indeed , we shall show that the method which we use is a topologically - correct ...
... orbital ( solid line ) composed of hybrid boron orbitals ( broken lines ) show that this similarity arises from topological aspects of the problem ; indeed , we shall show that the method which we use is a topologically - correct ...
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