¹H and ¹³C NMR assignments of the three dicyclopenta-fused pyrene congeners

Publication date

2006

Authors

Otero-Lobato, M.J.
van Walree, Cornelis AISNI 0000000389505154
Havenith, R.W.A.ISNI 0000000387541338
Jenneskens, LeoISNI 000000038742772X
Fowler, P.W.
Steiner, E.

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Article
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Abstract

Complete ¹H and ¹³HC NMR assignments of the (di-)cyclopenta-fused pyrene congeners, cyclopenta[cd]- (2), dicyclopenta[cd,fg]- (3), dicyclopenta[cd,jk]- (4) and dicyclopenta[cd,mn]pyrene (5), respectively, are archieved using two-dimensional (2D) NMR spectroscopy. The experimental ¹³C chemical shift assignments are compared with computed ab initio CTOCD-PZ2/6-31G** ¹³C chemical shifts; a satisfactory agreement is found. Substituent-induced chemical shifts in the pyrene core induced by annelation of cyclopenta moieties are discussed. Effects of dicyclopenta topology on electric structure are illustrated for 3-5.

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Citation

Otero-Lobato, M J, van Walree, C A, Havenith, R W A, Jenneskens, L W, Fowler, P W & Steiner, E 2006, '¹H and ¹³C NMR assignments of the three dicyclopenta-fused pyrene congeners', Tetrahedron, vol. 62, pp. 5510-5518.