Organic vapor sorption in a high surface area dysprosium(III)-phosphine oxide coordination material


Por: Ibarra I.A., Yoon J.W., Chang J.-S., Lee S.K., Lynch V.M., Humphrey S.M.

Publicada: 1 ene 2012
Resumen:
PCM-16 is a phosphine coordination material comprised of Dy(III) and triphenylphosphine oxide, which displays the highest reported CO 2 BET surface area for a Ln(III) coordination polymer of 1511 m 2 g -1. PCM-16 also adsorbs 2.7 wt % H 2 and 65.1 wt % O 2 at 77 K and 0.97 bar. The adsorption-desorption behavior of a series of organic vapors has been studied in PCM-16 to probe the nature of certain host-guest interactions in the pores. Aromatic and polar guest species showed high uptakes and marked adsorption/desorption hysteresis, while aliphatic vapors were less easily adsorbed. The surface area of PCM-16 could be increased significantly (to 1814 m 2 g -1) via exchange of Me 2NH 2 + cations in the pores with smaller NH 4 + groups. © 2012 American Chemical Society.

Filiaciones:
Ibarra I.A.:
 Department of Chemistry and Biochemistry, University of Texas at Austin, 1 University Station A5300, Austin, TX 78712-0165, United States

Yoon J.W.:
 Catalysis Center for Molecular Engineering, Korea Research Institute of Chemical Technology, P.O. Box 107, Yusung, Daejeon, 305-600, South Korea

Chang J.-S.:
 Catalysis Center for Molecular Engineering, Korea Research Institute of Chemical Technology, P.O. Box 107, Yusung, Daejeon, 305-600, South Korea

Lee S.K.:
 Catalysis Center for Molecular Engineering, Korea Research Institute of Chemical Technology, P.O. Box 107, Yusung, Daejeon, 305-600, South Korea

Lynch V.M.:
 Department of Chemistry and Biochemistry, University of Texas at Austin, 1 University Station A5300, Austin, TX 78712-0165, United States

Humphrey S.M.:
 Department of Chemistry and Biochemistry, University of Texas at Austin, 1 University Station A5300, Austin, TX 78712-0165, United States
ISSN: 00201669
Editorial
AMER CHEMICAL SOC, 1155 16TH ST, NW, WASHINGTON, DC 20036 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 51 Número: 22
Páginas: 12242-12247
WOS Id: 000311173700020
ID de PubMed: 23116537

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