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  • Title: Can a Cl-H···F Hydrogen Bond Replace a Cl···F Halogen Bond? H2XP:ClY:ZH versus H2XP:ClY:HZ for Y, Z = F, Cl.
    Author: Del Bene JE, Alkorta I, Elguero J.
    Journal: J Phys Chem A; 2019 May 09; 123(18):3992-3999. PubMed ID: 31032609.
    Abstract:
    Ab initio MP2/aug'-cc-pVTZ (where MP2 is Møller-Plesset perturbation theory) calculations have been carried out on four series of complexes, H2XP:ClF:HCl, H2XP:ClF:HF, H2XP:ClCl:HF, and H2XP:ClCl:HCl, to answer the question raised in the title of this paper. When X is F or Cl, binary complexes containing a P(V) molecule hydrogen bonded to an acid are found on all potential surfaces except H2ClP:ClF:HF, where an ion-pair complex exists. Ion-pair complexes also result from the optimization of H2XP:ClF:HF for X = NC, CN, and H. Changing the central molecule from ClF to ClCl has a dramatic effect on the nature of the optimized complexes when the substituents are NC, CN, and H. On the potential surfaces H2XP:ClCl:FH for X = NC and CN, open ternary complexes stabilized by a pnicogen bond and a hydrogen bond are found. Optimization of H3P:ClCl:FH leads to an ion pair. For H2(NC)P:ClCl:HCl and H2(CN)P:ClCl:HCl, cyclic ternary complexes stabilized by pnicogen, halogen, and hydrogen bonds result from optimization. Optimization of H3P:ClCl:HCl leads to a reaction in which H2ClP and a second HCl molecule are formed, and the resulting cyclic ternary complex is stabilized by two hydrogen bonds and a pnicogen bond. Thus, the type of complex resulting from the optimization of the starting ternary complex H2XP:ClY:HZ depends on the nature of the central molecule ClF or ClCl, the terminal molecule HCl or HF, and the substituent X. It is not possible to simply turn around the terminal HZ molecule in complexes H2XP:ClF:ZH for Z = F and Cl to give H2XP:ClF:HZ, thereby replacing a halogen bond by a hydrogen bond. Complexes H2XP:ClCl:HZ for X = NC and CN are stable complexes, but the corresponding halogen-bonded complexes H2XP:ClCl:ZH are not.
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