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