@article {3742,
	title = {On the conformational analysis and photochemical reactivity of 1,6-cyclodecanedione},
	journal = {Molecular Crystals and Liquid Crystals Science and Technology Section a-Molecular Crystals and Liquid Crystals},
	volume = {276},
	year = {1996},
	note = {ISI Document Delivery No.: UJ432Times Cited: 0Cited Reference Count: 2712th International Conference on the Chemistry of the Organic Solid State (ICCOSS XII)JUL 09-14, 1995MATSUYAMA, JAPANMinist Educ, Japan, Ehime Univ, Chem Soc Japan, Soc Synthet Organ Chem, Japan},
	pages = {A289-A298},
	type = {Proceedings Paper},
	abstract = {Photolysis of 1,5-cyclodecanedione, both in the crystalline state and in solution, fails to lead to any Norrish/Yang type II products despite the fact that the conformation of the molecule in the solid state is nearly ideal for hydrogen atom abstraction. Based on X-ray crystal structure and molecular modeling studies, it is argued that gamma-hydrogen abstraction does occur in the solid state, but that closure of the resulting 1,4-biradical is slower than reverse hydrogen atom transfer owing to difficulty in forming the expected 8-membered ring-containing photoproduct. In solution, on the other hand, molecular mechanics calculations indicate that the lack of photoreactivity of 1,5-cyclodecanedione stems from the fact that this molecule exists nearly exclusively in a conformation for which gamma-hydrogen abstraction is sterically impossible.},
	keywords = {ABSTRACTION, C-H...O, II REACTIONS, KETONES, MOLECULAR MECHANICS METHODOLOGY},
	isbn = {1058-725X},
	url = {<Go to ISI>://A1996UJ43200083},
	author = {Lewis, T. J. and Rettig, S. J. and Sauers, R. R. and Scheffer, J. R. and Trotter, J. and Wu, C. H.}
}
@article {3742,
	title = {On the conformational analysis and photochemical reactivity of 1,6-cyclodecanedione},
	journal = {Molecular Crystals and Liquid Crystals Science and Technology Section a-Molecular Crystals and Liquid Crystals},
	volume = {276},
	year = {1996},
	note = {ISI Document Delivery No.: UJ432Times Cited: 0Cited Reference Count: 2712th International Conference on the Chemistry of the Organic Solid State (ICCOSS XII)JUL 09-14, 1995MATSUYAMA, JAPANMinist Educ, Japan, Ehime Univ, Chem Soc Japan, Soc Synthet Organ Chem, Japan},
	pages = {A289-A298},
	type = {Proceedings Paper},
	abstract = {Photolysis of 1,5-cyclodecanedione, both in the crystalline state and in solution, fails to lead to any Norrish/Yang type II products despite the fact that the conformation of the molecule in the solid state is nearly ideal for hydrogen atom abstraction. Based on X-ray crystal structure and molecular modeling studies, it is argued that gamma-hydrogen abstraction does occur in the solid state, but that closure of the resulting 1,4-biradical is slower than reverse hydrogen atom transfer owing to difficulty in forming the expected 8-membered ring-containing photoproduct. In solution, on the other hand, molecular mechanics calculations indicate that the lack of photoreactivity of 1,5-cyclodecanedione stems from the fact that this molecule exists nearly exclusively in a conformation for which gamma-hydrogen abstraction is sterically impossible.},
	keywords = {ABSTRACTION, C-H...O, II REACTIONS, KETONES, MOLECULAR MECHANICS METHODOLOGY},
	isbn = {1058-725X},
	url = {<Go to ISI>://A1996UJ43200083},
	author = {Lewis, T. J. and Rettig, S. J. and Sauers, R. R. and Scheffer, J. R. and Trotter, J. and Wu, C. H.}
}
@article {7308,
	title = {CRYSTALLOGRAPHIC DETERMINATION OF THE PREFERRED GEOMETRY FOR INTRAMOLECULAR HYDROGEN-ATOM ABSTRACTION IN 1,8-CYCLOHEXADECANEDIONE},
	journal = {Molecular Crystals and Liquid Crystals},
	volume = {219},
	year = {1992},
	note = {ISI Document Delivery No.: JD451Times Cited: 6Cited Reference Count: 2410TH INTERNATIONAL CONF ON THE CHEMISTRY OF THE ORGANIC SOLID STATE ( ICCOSS 10 )JUL 07-12, 1991VANCOUVER, CANADACHEM INST CANADA, NAT SCI \& ENGN RES COUNCIL CANADA, PETR RES FUND, UNIV BRIT COLUMBIA, BRUKER SPECTROSPIN CANADA, CHEMAGNETICS, DOTY SCI, GORDON \& BREACH SCI PUBL},
	pages = {17-28},
	type = {Proceedings Paper},
	keywords = {CRYSTAL STRUCTURE-REACTIVITY, HYDROGEN ABSTRACTION GEOMETRY, II REACTIONS, MACROCYCLIC DIKETONE, MOLECULAR MECHANICS METHODOLOGY, NORRISH TYPE-II REACTION, PHOTOCHEMISTRY, REACTIVITY, RELATIONSHIPS, SOLID STATE ORGANIC PHOTOCHEMISTRY, STATE, TRANSFERS, TRANSITION STRUCTURES},
	isbn = {0140-6566},
	url = {<Go to ISI>://A1992JD45100002},
	author = {Lewis, T. J. and Rettig, S. J. and Scheffer, J. R. and Trotter, J.}
}
@article {7308,
	title = {CRYSTALLOGRAPHIC DETERMINATION OF THE PREFERRED GEOMETRY FOR INTRAMOLECULAR HYDROGEN-ATOM ABSTRACTION IN 1,8-CYCLOHEXADECANEDIONE},
	journal = {Molecular Crystals and Liquid Crystals},
	volume = {219},
	year = {1992},
	note = {ISI Document Delivery No.: JD451Times Cited: 6Cited Reference Count: 2410TH INTERNATIONAL CONF ON THE CHEMISTRY OF THE ORGANIC SOLID STATE ( ICCOSS 10 )JUL 07-12, 1991VANCOUVER, CANADACHEM INST CANADA, NAT SCI \& ENGN RES COUNCIL CANADA, PETR RES FUND, UNIV BRIT COLUMBIA, BRUKER SPECTROSPIN CANADA, CHEMAGNETICS, DOTY SCI, GORDON \& BREACH SCI PUBL},
	pages = {17-28},
	type = {Proceedings Paper},
	keywords = {CRYSTAL STRUCTURE-REACTIVITY, HYDROGEN ABSTRACTION GEOMETRY, II REACTIONS, MACROCYCLIC DIKETONE, MOLECULAR MECHANICS METHODOLOGY, NORRISH TYPE-II REACTION, PHOTOCHEMISTRY, REACTIVITY, RELATIONSHIPS, SOLID STATE ORGANIC PHOTOCHEMISTRY, STATE, TRANSFERS, TRANSITION STRUCTURES},
	isbn = {0140-6566},
	url = {<Go to ISI>://A1992JD45100002},
	author = {Lewis, T. J. and Rettig, S. J. and Scheffer, J. R. and Trotter, J.}
}
