Fluorescence of A100 MOF and Adsorption of Water, Indole, and Naphthalene on A100 by the Spectroscopic, Kinetic, and DFT Studies

被引:22
作者
Dai, Jun [1 ]
McKee, Michael L. [2 ]
Samokhvalov, Alexander [1 ]
机构
[1] Rutgers State Univ, Dept Chem, Camden, NJ 08102 USA
[2] Auburn Univ, Dept Chem & Biochem, Auburn, AL 36849 USA
关键词
METAL-ORGANIC FRAMEWORKS; LIQUID-PHASE; THERMOCHEMICAL KINETICS; DENSITY FUNCTIONALS; NITROGEN-COMPOUNDS; ACTIVE-SITES; SEPARATION; MOLECULES; DENITROGENATION; DESULFURIZATION;
D O I
10.1021/jp510272s
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Metalorganic frameworks (MOFs) are promising materials for adsorption and separations. It is important to understand the details of chemical bonding between the adsorbate and structural units in the MOFs. In A100 MOF, the near-UVvisible fluorescence is found to be the intralinker fluorescence. Naphthalene and indole form the stoichiometric host-guest pp adsorption complexes with A100 that contain one adsorbate molecule per two BDC linkers, and adsorption of indole causes a strong quenching of the intralinker fluorescence. The excitation wavelength dependent steady-state fluorescence spectra, the nanosecond time-resolved fluorescence spectra, and DFT calculations indicate the strong pp interactions between adsorbed indole and naphthalene and aromatic ring of the BDC linker, as well as hydrogen bonding between adsorbed indole and COO group of the linker. Activated A100 adsorbs up to four water molecules per BDC linker. Kinetic study of adsorption of naphthalene and indole from n-alkane on hydrated A100 yields the preferential adsorption of indole as determined by the in-situ time-dependent fluorescence spectroscopy and complementary ex-situ UVvis absorption spectroscopy.
引用
收藏
页码:2491 / 2502
页数:12
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