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Structural response to desolvation in a pyridyl-phenanthrene diarylethene-based metal-organic framework

  • Ian M. Walton
  • , Jordan M. Cox
  • , Travis B. Mitchell
  • , Nicholas P. Bizier
  • , Jason B. Benedict
  • SUNY Buffalo
  • Daemen College

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

A phenanthrene-based diarylethene linker with linear pyridyl connectivity, 4,4′-(9,10-bis(2,5-dimethylthiophen-3-yl)phenanthrene-2,7-diyl)dipyridine linker (TPDPy) was prepared and subsequently used to synthesize an air-stable metal-organic framework, UBMOF-3 (Zn3(BDC)3(TPDPy)1(DMF)1.5, BDC = 1,4-benzenedicarboxylate, DMF = N,N-dimethylformamide). Upon irradiation with ultraviolet light, this photo-responsive framework, composed of terephthalate, TPDPy, and zinc pinwheels, exhibits strong linear dichroism consistent with the crystal structure. Activation (desolvation) of the crystal leads to a significant change in the crystal structure that improves the ability to crystallographically resolve the photochromic linker.

Original languageEnglish
Pages (from-to)7972-7977
Number of pages6
JournalCrystEngComm
Volume18
Issue number41
DOIs
StatePublished - 2016

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