RESONANCE-ASSISTED HYDROGEN-BONDING .3. FORMATION OF INTERMOLECULAR HYDROGEN-BONDED CHAINS IN CRYSTALS OF BETA-DIKETONE ENOLS AND ITS RELEVANCE TO MOLECULAR ASSOCIATION

Citation
G. Gilli et al., RESONANCE-ASSISTED HYDROGEN-BONDING .3. FORMATION OF INTERMOLECULAR HYDROGEN-BONDED CHAINS IN CRYSTALS OF BETA-DIKETONE ENOLS AND ITS RELEVANCE TO MOLECULAR ASSOCIATION, Acta crystallographica. Section B, Structural science, 49, 1993, pp. 564-576
Citations number
81
Categorie Soggetti
Crystallography
ISSN journal
01087681
Volume
49
Year of publication
1993
Part
3
Pages
564 - 576
Database
ISI
SICI code
0108-7681(1993)49:<564:RH.FOI>2.0.ZU;2-G
Abstract
The beta-diketone enol (or enolone) HO-C=C-C=O fragment produced by en olization of beta-diketones is known to form strong intramolecular O-H ...O hydrogen bonds where the decrease of the O...O contact distance ( up to 2.40 angstrom) is correlated with the increased pi-delocalizatio n of the O-C=C-C=O heteroconjugated system, the phenomenon has been in terpreted by the resonance-assisted hydrogen-bonding (RAHB) model [Gil li, Bellucci, Ferretti & Bertolasi (1989). J. Am. Chem. Soc. 111. 1023 -1028; Bertolasi, Gilli, Ferretti & Gilli (1991). J. Am. Chem. Soc. 11 3, 4917-4925]. When the intramolecular hydrogen bond is forbidden for steric reasons, molecules crystallize by forming hydrogen-bonded infin ite chains of pi-delocalized enolone fragments (resonant beta-chains), i.e. they are hybrids of the canonical forms -OH...O=C-C=C-OH...O=C- <-- --> =+OH...-O-C=C-C=+OH...-O-C=. The occurrence of beta-chains in 14 crystals of enolone (2-en-3-ol-1-one) and eight of enediolone (2-en -2,3-diol-1-one) derivatives has been studied. The beta-chains were fo und to have the following properties: (i) O...O distances depend on th e enediolone substituents and range from 2.69 angstrom in beta-ketoest ers to 2.46 angstrom in beta-diketones; (iii) calculated hydrogen-bond energies are in the range 20-66 kJ mol-1; (iii) a strict intercorrela tion between hydrogen-bond strengthening and pi-system delocalization is observed, in complete agreement with the RAHB model proposed previo usly. Beta-Chain morphologies are analyzed with the aim of determining crystal-engineering rules for the production of solid materials where systems of polar beta-chains can induce ferroelectric and second harm onic generation properties. The RAHB concept is generalized to other h eteroconjugated systems such as carboxylic acids, amides, enamines (RN =CR-NHR) and enaminones (O=CR-CR=CR-NHR), and its possible relevance i n biological processes such as base coupling in DNA and folding of pro teins is briefly discussed.