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Hydrogen Bonding and Lewis Acid–Base Interactions in the System Bis(pentafluorophenyl)borinic Acid / Methanol
Author(s) -
Donghi Daniela,
Maggioni Daniela,
Beringhelli Tiziana,
D'Alfonso Giuseppe,
Mercandelli Pierluigi,
Sironi Angelo
Publication year - 2008
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200701210
Subject(s) - chemistry , adduct , hydrogen bond , dimer , lewis acids and bases , monomer , medicinal chemistry , covalent bond , polymer chemistry , stereochemistry , organic chemistry , molecule , catalysis , polymer
Methanol does not significantly affect the position and the rate of the equilibrium between the monomeric ( 1 m ) and cyclic trimeric ( 1 t ) forms of bis(pentafluorophenyl)borinic acid, Ar 2 BOH ( 1 , Ar = C 6 F 5 ), in CD 2 Cl 2 solution. This contrasts with what was previously observed in the presence of thf and is mainly due to the stabilization of the 1 m · MeOH covalent adduct through the formation of the hydrogen‐bonded dimer [Ar 2 B(OH)(MeOH)] 2 ( 7 ), characterized in solution and by single‐crystal X‐ray analysis. This dimer can be viewed as the intermediate in the conversion of 1 into its methyl ester 6 by fast proton transfer along the hydrogen bond, which transforms the 1 m · MeOH adduct into the 6· H 2 O adduct. Extrusion of H 2 O by water scavengers drives the equilibrium toward ester 6 . X‐ray analysis showed that, at variance with 1 , ester 6 in the solid state is a monomer. Hindered rotation [Δ H # = 38(1) kJ mol –1 , Δ S # = –35(6) J mol –1 ] around the B–OMe bond, due to O‐to‐B π‐donation, has been observed. This π‐donation lowers the Lewis acidity of 6 , as shown by the thermal instability of its adducts with MeOH and thf. Water addition to 6 affords the dimeric adduct 7 , in fast equilibrium with both 1 m and 6 , even at 183 K, as revealed by 2D EXSY analysis. Borinic acid itself can act as a water scavenger at low temperature, so that 6 is formed also in the early stages of the titration of 1 with MeOH. The other main initial product was the adduct [Ar 2 B(OH)] 3 · MeOH ( 3 ) containing a MeOH molecule bound within an octaatomic –B–O(H)–B–O(Me)–H ··· O(H)–B–O(H)– ring. Fast proton transfer along the strong hydrogen bond was revealed by 2D EXSY analysis. At variance with thf, the adduct containing MeOH exocyclically hydrogen‐bonded to 1 t could be obtained in high concentration at 183 K only when due allowance for the kinetic requirements of the slow trimerization equilibrium was made.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)