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Title: Structure, Dynamics, and Photophysics in the Copper(I) Iodide–Tetrahydrothiophene System

Journal Article · · Crystal Growth and Design
DOI:https://doi.org/10.1021/cg500005p· OSTI ID:1385702
 [1];  [1];  [1];  [2];  [2];  [2];  [3];  [3]
  1. Department of Chemistry, College of William and Mary, Williamsburg, Virginia 23187-8795, United States
  2. Department of Chemistry, University of Maine, Orono, Maine 04469-5706, United States
  3. Department of Chemistry, The George Washington University, Washington, D.C. 20052, United States

Combination of CuI and tetrahydrothiophene (THT) in MeCN or neat THT produces various phases, depending upon experimental conditions. Green luminescent product (CuI)4(THT)2 (1) consists of Cu4I4 cubane units knit into a 3-D network by μ2-THT ligands. Dull yellow luminescent (CuI)10(THT)7(MeCN) (2) contains {[Cu4I4(THT)](μ2-THT)2(Cu2I2)(μ2-THT)2[Cu4I4(NCMe)]} “rungs” linked into 1-D ladders by pairs of μ2-THT ligands. Two molecular (CuI)4(THT)4 phases were found: orange luminescent 3a and yellow luminescent 3b. Triclinic 3b is the more stable phase at 25 °C, but it undergoes endothermic transformation to monoclinic 3a at 38 °C. Compound 3a transforms to a triclinic phase (3a') that retains orange emission at -60 °C. Nonemissive (CuI)3(THT)3·MeCN (4) is a 2-D sheet structure in which Cu3(THT)3 rings are linked in trigonal directions by rhomboid Cu2I2 dimer units. The previously reported (CuI)2(THT)4 (5) is a molecular dimer. Temperature and mixing ratio domains for the formation of the CuI–THT phases from MeCN are presented. Luminescence in 1, 2, 3a, and 3b is rationalized on the basis of varying degrees of halide-to-metal charge transfer (XMCT) and metal-centered (MC) behavior. Low-temperature spectra reveal reversible changes, including modest red shifts for 1 and 2, and splitting into two excitation/emission band pairs for 3a and 3b.

Research Organization:
Energy Frontier Research Centers (EFRC) (United States). Materials Science of Actinides (MSA)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
DOE Contract Number:
SC0001089
OSTI ID:
1385702
Journal Information:
Crystal Growth and Design, Vol. 14, Issue 3; Related Information: MSA partners with University of Notre Dame (lead); University of California, Davis; Florida State University; George Washington University; University of Michigan; University of Minnesota; Oak Ridge National Laboratory; Oregon state University; Rensselaer Polytechnic Institute; Savannah River National Laboratory; ISSN 1528-7483
Publisher:
American Chemical Society
Country of Publication:
United States
Language:
English