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8 matching references were found.
Santiago, C.; Houk, K.N.; DeCicco, G.J.; Scott, L.T., The photoelectron and ultraviolet spectra of octamethylcyclododeca-1,3,7,9-tetrayne: a weakly antiaromatic molecule, J. Am. Chem. Soc., 1978, 100, 692. [all data]
Scott, L.T.; Erden, I.; Brunsvold, W.R.; Schultz, T.H.; Houk, K.N.; Paddon-Row, M.N., Competitive [6 + 2], [4 + 2], and [2 + 2] cycloadditions. Experimental classification of two-electron cycloaddends, J. Am. Chem. Soc., 1982, 104, 3659. [all data]
Houk, K.N.; Scott, L.T.; Rondan, N.G.; Spellmeyer, D.C.; Reinhardt, G.; Hyun, J.L.; DeCicco, G.J.; Weiss, R.; Chen, M.H.M.; Bass, L.S.; Clardy, J.; Jorgensen, F.S.; Eaton, T.A.; Sarkozi, V.; Petit, C.M., Pericyclynes: 'Exploded cycloalkanes' with unusual orbital interactions and conformational properties. MM2 and STO-3G calculations, x-ray crystal structures, photoelectron spectra, and electron transmission spectra, J. Am. Chem. Soc., 1985, 107, 6556. [all data]
Scott, L.T.; Cooney, M.J.; Rogers, D.W.; Dejroongruang, K., Homoaromaticity in a cyclic polyacetylene, J. Am. Chem. Soc., 1988, 110, 7244-7245. [all data]
Kiyobayashi, T.; Nagano, Y.; Sakiyama, M.; Yamamoto, K.; Cheng, P.-C.; Scott, L.T., Formation enthalpy of corannulene: Microbomb combustion calorimetry, J. Am. Chem. Soc., 1995, 117, 3270-3271. [all data]
Chen, G.; Cooks, R.G.; Corpuz, E.; Scott, L.T., Estimation of the Electron Affinities of C60, Corannulene, and Coronene by Using the Kinetic Method, J. Am. Soc. Mass Spectrom., 1996, 7, 7, 619, https://doi.org/10.1016/1044-0305(96)85610-8 . [all data]
Chen, G.; Ma, S.; Cooks, R.G.; Bronstein, H.E.; Best, M.D.; Scott, L.T., Electron Affinities and C60 Anion Clusters of Certain Bowl-shaped Polycyclic Aromatic Hydrocarbons, J. Mass Spectrom., 1997, 32, 12, 1305, https://doi.org/10.1002/(SICI)1096-9888(199712)32:12<1305::AID-JMS590>3.0.CO;2-W . [all data]
Prinzbach, H.; Weller, A.; Landenberger, P.; Wahl, F.; Worth, J.; Scott, L.T.; Gelmont, M.; Olevano, D.; von I., Gas-phase production and photoelectron spectroscopy of the smallest fullerene, C-20, Nature, 2000, 407, 6800, 60-63, https://doi.org/10.1038/35024037 . [all data]