Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 11 December 1992:
Vol. 258. no. 5089, pp. 1769 - 1772
DOI: 10.1126/science.258.5089.1769

Articles

Open Framework Structures Based on Sex2– Fragments: Synthesis of (Ph4P)[M(Se6)2] (M = Ga, In, TI) in Molten (Ph4P)2Sex

Sandeep Dhingra 1 and Mercouri G. Kanatzidis 1

1 Department of Chemistry and Center for Fundamental Materials Research, Michigan State University, East Lansing, MI 48824

Polychalcogenide compounds with open polymeric frameworks are rare, and they represent a class of compounds in which microporosity might be achieved. Microporous frameworks that are not oxide-based are now attracting interest because of the combination of catalytic and electronic properties they may simultaneously possess. Three new compounds that may be forerunners to such materials have been discovered and are reported here. The reaction of gallium (Ga), indium (In), and thallium (TI) metal with (Ph4P)2Se5 (Ph, phenyl) and an excess of elemental selenium (Se) in a sealed, evacuated Pyrex tube at 200°C yielded small red crystals of (Ph4P)[Ga(Se6)2] (I), (Ph4P)[In(Se6)2] (II), and (Ph4P)[TI(Se6)2] (III), respectively. The [M(Se6)2] (M = Ga, In, TI) ions form a two-dimensional, open framework filled with Ph4P+ ions. The [M(Se6)2]nn– structure consists of tetrahedral M3+ centers and bridging Se62– ligands, leading to an extended structure in two dimensions. These layers stack perfectly one on top of the other giving rise to one-dimensional channels running down the c axis that are filled with Ph4P+ cations. These cations are situated in the layers, as opposed to between the layers, and the whole structure can be viewed as a template. Compound II shows remarkable thermal stability and melts congruently at 242°C. Upon cooling to room temperature it gives a glassy phase that recrystallizes upon subsequent heating to 160°C.

Submitted on July 2, 1992
Accepted on October 9, 1992


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Microporous and Photoluminescent Chalcogenide Zeolite Analogs.
N. Zheng, X. Bu, B. Wang, and P. Feng (2002)
Science 298, 2366-2369
   Abstract »    Full Text »    PDF »
Supertetrahedral Sulfide Crystals with Giant Cavities and Channels.
H. Li, A. Laine, M. O'Keeffe, and O. M. Yaghi (1999)
Science 283, 1145-1147
   Abstract »    Full Text »
Turning Down the Heat: Design and Mechanism in Solid-State Synthesis.
A. Stein, S. W. Keller, and T. E. Mallouk (1993)
Science 259, 1558-1564
   Abstract »    PDF »



ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)