Studies on the trapping and detrapping transition states of atomic hydrogen in octasilsesquioxane using the density functional theory B3LYP method

Michiko Mattori, Koichi Mogi

    Research output: Contribution to journalArticle

    25 Citations (Scopus)

    Abstract

    B3LYP level optimizations were performed on the structures of the octasilsesquioxane (Si8O12H8, HT8) double four-ring (D4R) cage and single hydrogen atom-trapped HT8 (H@HT8). Moreover, the transition state in the detrapping process of the hydrogen atom from the D4R cage was examined. The basis sets used were 6-31G** for HT8 and (311/1*1*/1*) for the trapped hydrogen atom. Both HT8 and H@HT8 were structure-optimized with Oh molecular symmetry and the resulting cage conformations were similar. The trapped H atom was located at the center of the D4R cage. The weak interaction between the D4R cage and the trapped H atom in H@HT8 was determined by examining the singly occupied molecular orbital (SOMO) [8a1g] of H@HT8. The SOMO was constructed from an antibonding interaction between the lowest unoccupied molecular orbital (LUMO) [8a1g] of HT8 and the 1s orbital of the trapped H atom. For the transition state, the structure was optimized with C4v molecular symmetry. As a result, the position of the Si8 cube framework was unchanged, and four O atoms in a silicon single four-ring were displaced, thereby opening one of the oxygen windows of the D4R cage. The detrapping H atom was located near the center of the oxygen window and the MO illustrations showed a change in shape from spherical to ellipsoid. Consequently, it is clear that the detrapping process is not due to the formation of chemical bonding. The calculated activation and reaction energies of this detrapping process were +98.6 and -26.1 kJ/mol, respectively. In addition, single-point calculations at the MP2 level were done for each optimized structure, and the obtained activation and reaction energies were + 128.7 and -9.3 kJ/mol, respectively. Both calculated activation energies were comparable to Stosser's experimental data (+109.6 ± 3.1 kJ/mol) for H·:Si8O12(OSi(CH3)3) 8 (Q8M8). Furthermore, additional explanations are given on the IR vibrational frequencies of HT8 and H@HT8 and the hyperfine coupling constant for caged atomic hydrogen by ESR.

    Original languageEnglish
    Pages (from-to)10868-10872
    Number of pages5
    JournalJournal of Physical Chemistry A
    Volume104
    Issue number46
    DOIs
    Publication statusPublished - Nov 23 2000

    All Science Journal Classification (ASJC) codes

    • Physical and Theoretical Chemistry

    Fingerprint Dive into the research topics of 'Studies on the trapping and detrapping transition states of atomic hydrogen in octasilsesquioxane using the density functional theory B3LYP method'. Together they form a unique fingerprint.

  • Cite this