44 results on '"Smith, Kevin"'
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2. New molten metal catalysts for CO2 and CH4 conversion to 2 : 1 H2 : CO syngas.
3. Metal-based chirality and spin state change in 16-electron CpML2 systems: a computational study of CpW(NO)(PH3)
4. Nitration of iron corrolates: further evidence for non-innocence of the corrole ligand
5. Functionalization of the corrole ring: the role of isocorrole intermediates
6. 6-Azahemiporphycene: a further example of corrole metamorphosis
7. b-Bilene to a,c-biladiene transformation during syntheses of isoporphyrins and porphyrins
8. Benzoporphyrins via an olefin ring-closure metathesis methodology
9. Cyclopentadienyl benzamidinato chromium complexes as models for alkyl halide activation by chromium reagentsElectronic supplementary information (ESI) available: experimental and computational details. See http://www.rsc.org/suppdata/cc/b2/b207710h/
10. A novel synthetic route to fused propenochlorin and benzochlorin photodynamic therapy probes
11. β,β′-Fused metallocenoporphyrinsElectronic supplementary information (ESI) available: molecular structure of 10. See http://www.rsc.org/suppdata/cc/b1/b107732e/
12. First structural characterization of a covalently bonded porphyrin–carborane system
13. Cr(NAr)(O)(NPri2)(Ar): a strongly-bent monoimido complex resulting from nitrosyl ligand cleavage
14. Synthesis and characterization of a chiral nonplanar porphyrin
15. Evidence for unusually strong intramolecular hydrogen bonding in highly nonplanar porphyrins
16. Synthesis and unusual properties of the first 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetraalkylporphyrin
17. Oligomeric porphyrin arrays
18. 5,10,15-Triphenylcorrole: a product from a modified Rothemund reaction
19. Novel products from bromination reactions of 5,10,15,20-tetraisopropylporphyrins
20. Cruciform porphyrin pentamers
21. Phosphorus complex of corrole
22. Stabilization of neutral oxophlorin π-radicals by bulky meso-alkyl groups
23. Rational approach to the synthesis of meso–meso (5,5′) linked bis-porphyrins
24. Synthesis of polyfunctionalized thiophenes and enediynes via ring-opening reactions of 3-lithiated thieno[2,3-b](and [3,2-b])thiophenes, 3,4-dilithiated thieno[2,3-b]thiophenes and 3,6-dilithiated thieno[3,2-b]thiophenes
25. New chemistry of porphyrin β-ketoesters: synthesis of a novel covalently-linked dimer
26. Steric control of tautomerism in tetrapyrroles: iso-oxophlorins
27. A convenient synthesis of functionalized tetraphenylchlorins
28. Direct meso-alkylation of meso-formylporphyrins using Grignard reagents
29. First syntheses of fused pyrroloporphyrins
30. Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity.
31. Oligomeric porphyrin arrays
32. Benzoporphyrins viaan olefin ring-closure metathesis methodologyElectronic supplementary information (ESI) available: General procedure and selected characterization data for porphyrins 11–13, 16and 17. See DOI: 10.1039/b607711k
33. Metal-based chirality and spin state change in 16-electron CpML2 systems: a computational study of CpW(NO)(PH3)
34. Conformational landscape surfing induced by offon ππ stacking in a porphyrinquinone dyad
35. β,β'-Fused metallocenoporphyrins
36. First structural characterization of a covalently bonded porphyrincarborane system
37. Cruciform porphyrin pentamers
38. Synthesis and unusual properties of the first 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetraalkylporphyrin
39. Evidence for unusually strong intramolecular hydrogen bonding in highly nonplanar porphyrins
40. Novel products from bromination reactions of 5,10,15,20-tetraisopropylporphyrins
41. Rational approach to the synthesis of meso–meso (5,5′) linked bis-porphyrins
42. New chemistry of porphyrin β-ketoesters: synthesis of a novel covalently-linked dimer
43. Synthesis of polyfunctionalized thiophenes and enediynes via ring-opening reactions of 3-lithiated thieno[2,3-b](and [3,2-b])thiophenes, 3,4-dilithiated thieno[2,3-b]thiophenes and 3,6-dilithiated thieno[3,2-b]thiophenes
44. Stabilization of neutral oxophlorin π-radicals by bulky meso-alkyl groups
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