Stella Ikuzwe

ORCID: 0000-0003-2113-3374
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About
Contact & Profiles
Research Areas
  • Luminescence and Fluorescent Materials
  • Organic Electronics and Photovoltaics
  • Photochromic and Fluorescence Chemistry
  • Synthesis and biological activity
  • Nonlinear Optical Materials Research
  • Conducting polymers and applications

Macalester College
2019

This work describes a three-step chromatography-free protocol for the synthesis of novel organic materials building block, dichlorinated mellophanic diimide (MDI), that is shown to undergo nucleophilic substitution with variety ortho disubstituted benzenes yield series chromophores. Furthermore, 1,2,4,5-tetrasubstituted can be used synthesize tetraimide heteropentacene derivatives endcapped by MDI motifs. The fine-tuning effects heteroatom identity were investigated UV–vis and fluorescence...

10.1021/acs.joc.9b01502 article EN The Journal of Organic Chemistry 2019-07-18

This work describes a three-step chromatography-free protocol for the synthesis of novel organic materialsbuilding block, dichlorinated mellophanic diimide (MDI), that is shown to undergo nucleophilic substitutionwith variety ortho disubstituted benzenes yield series chromophores. Furthermore, 1,2,4,5-tetrasubstituted can be used synthesize tetraimide heteropentacene derivatives endcapped byMDI motifs. The fine-tuning effects heteroatom identity were investigated by UV-Vis and...

10.26434/chemrxiv.8236466.v1 preprint EN cc-by-nc-nd 2019-06-07

<div>This work describes a three-step chromatography-free protocol for the synthesis of novel organic materials</div><div>building block, dichlorinated mellophanic diimide (MDI), that is shown to undergo nucleophilic substitution</div><div>with variety ortho disubstituted benzenes yield series chromophores. Furthermore, 1,2,4,5-</div><div>tetrasubstituted can be used synthesize tetraimide heteropentacene derivatives endcapped...

10.26434/chemrxiv.8236466 preprint EN cc-by-nc-nd 2019-06-07
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