Full Length ArticleThermochemistry of hydrogen bonding of proton acceptors in the media of linear and cyclic amides. Cooperativity effects in multi-particle complexes of amides

- Enthalpies of solution were measured of 10 proton acceptor solute in amides.
- The solution of proton acceptor in self-associated amide leads to reorganization HB.
- The cooperative effect changes inversely from proton acceptor properties.

In present work a thermochemistry of hydrogen bond formation of proton acceptors (B) in the medium of linear (N-methylformamide (NMF)) and cyclic (2-pyrrolidone (Py)) amides was studied. The infinite dilution solution enthalpies of nitriles, ketones, esters, ethers and amines in amides were measured at 298.15 K. Enthalpies of hydrogen bonding of proton acceptors in solution linear and cyclic amides were calculated and compared with previously determined the enthalpies of hydrogen bonding of amides in proton acceptor media. The cooperative effects of hydrogen bonding in multi-particle complexes of amides with proton acceptors were evaluated. It was shown that cooperativity coefficients were decreased with increasing the basicity of proton acceptors.

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