Because polypeptides present a repeating sequence of amide bonds, lactams provide good model compounds for investigating the angular dependencies of coupling constants over a range of rigid conformations. A number of ¹³C labeled lactams were synthesized to cover a range of dihedral angles; experimental and theoretical carbon-carbon and carbon-hydrogen coupling constants were obtained to give the relationships between the vicinal coupling constants ³J[C(O)-N-C-C], ³J[C(O)-N-C-H] and dihedral angle φ. Vicinal ¹³C-¹³C coupling constants for dihedral angles in the range of 90° to 180° were obtained unambiguously from the coupling between the carbonyl and carbons in the side chains of lactams. However, due to coupling via multiple paths, vicinal ¹³C-¹³C coupling constants for dihedral angles ranging from 0° to 90° were estimated by excluding the contributions from the geminal ²J[C(O)-C-C] or vicinal ³J[C(O)-C-C-C] couplings in the lactam rings. The experimental and theoretical results show that the angular dependence of vicinal ¹³C-¹³C coupling constants do not follow a simple Karplus type relationship, especially at small dihedral angles. It was found that geminal ²J[C(O)-N-C] were small ( < 0.3 Hz). However, the ²J[C(O)-N-C] in the cis arrangement are shifted to about 2.2 Hz in N-methyl substituted lactams while in the trans arrangement the values are about 4.4 Hz. Geminal ¹³C-¹³C coupling constants ²J[(C(O)-N-C)] also provide a useful tool in stereochemical studies.

No description available.

Thesis (Ph. D.)--University of Missouri-Columbia, 2001. / Typescript. Vita. Includes bibliographical references (leaves 74-76). Also available on the Internet.

Thesis (Ph. D.)--University of Missouri-Columbia, 2001. / Typescript. Vita. Includes bibliographical references (leaves 74-76). Also available on the Internet.

No description available.

The results obtained by this new method are shown to be able to account for most of the shortcomings of the earlier methods, in particular their failure satisfactorily to explain the quenching of luminescence in cis-polyacetylene and their poor predictions of the relative strengths of the two photoinduced absorption peaks in polythiophene. The ability of trans-polyacetylene (t-PA) to support a novel type of dynamic defect known as a breather is also verified. A quantitative estimate is made of the mobility of the fundamental defect in t-PA, known as a soliton, and this is in good agreement with experiment.

Thesis (Ph.D.). / Written for the Dept. of Physics. Title from title page of PDF (viewed 2009/06/09). Includes bibliographical references.

Presented as Thesis (Ph. D.)--University of Wisconsin--Madison, 1911. / Cover title. Reprinted from Physical review, vol. 33 (Dec. 1911). Includes bibliographical references.

Thesis (M.S.)--Tennessee Technological University, 2008. / Title from title page screen (viewed on May 17, 2010). Bibliography: leaves 56-58.

No description available.