Glycylglycine π→π and Charge Transfer Transition Moment Orientations:  Near-Resonance Raman Single-Crystal Measurements

• Published in: Journal of the American Chemical Society 1996-10, Vol.118 (40), p.9716-9726
• Main Authors: Pajcini, Vasil, Chen, X. G, Bormett, Richard W, Geib, Steven J, Li, Pusheng, Asher, Sanford A, Lidiak, Edward G
• Format: Article
• Language: English
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja961725z

We have grown a novel crystal of hydrated gycylglycine (Gly-Gly), determined its crystal structure, and measured its Raman tensor at 488, and 244 nm, close to resonance. This crystal has 8 molecules of (Gly-Gly) and 12 molecules of water per unit cell. The Gly-Gly hydrogen-bonds in a β-sheet-like structure where all of the amide planes are parallel. We report here the development of a general method to use preresonance single-crystal Raman measurements to determine the direction of the molecular electronic transition moments. We utilize the UV (244 nm) excited Raman tensor and relationships derived here to accurately determine the transition moment orientation of the amide and carboxylate group π→π* transitions and the orientation of a charge transfer transition from the carboxylate group to the amide group. The amide π→π* (NV1) transition moment is found to be in the peptide plane at an angle of −46° ± 3° to the amide carbonyl bond. The carboxylate π→π* (NV1‘) transition moment is oriented almost parallel to a line connecting the carboxylate oxygens (4.6° off), as theoretically expected. The charge transfer band from the carboxylate to the amide chromophore is found at an angle of −83° ± 3° to the amide carbonyl bond, almost along the line of intersection of the amide and carboxylate planes.