Parker J. W. Sommerville

ORCID: 0000-0003-0699-4272
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About
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Research Areas
  • Organic Electronics and Photovoltaics
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Molecular Junctions and Nanostructures
  • Conducting polymers and applications
  • Organic Light-Emitting Diodes Research
  • Force Microscopy Techniques and Applications
  • Luminescence and Fluorescent Materials
  • Organometallic Complex Synthesis and Catalysis
  • Chemical Synthesis and Analysis
  • Ionic liquids properties and applications
  • Synthesis and Properties of Aromatic Compounds
  • Organoboron and organosilicon chemistry

University of Washington
2019-2024

Seattle University
2019-2021

California Polytechnic State University
2019

Indacenodithiophene (IDT) copolymers are a class of conjugated polymers that have limited long-range order and high hole mobilities, which makes them promising candidates for use in deformable electronic devices. Key to their mobilities is the coplanar monomer repeat units within backbone. Poly(indacenodithiophene-benzothiadiazole) (PIDTC16-BT) poly(indacenodithiophene-thiapyrollodione) (PIDTC16-TPDC1) two IDT with planar backbones, but they brittle at low molecular weight unsuitably elastic...

10.1021/acspolymersau.2c00034 article EN cc-by-nc-nd ACS Polymers Au 2022-09-29

Poly(indacenodithiophene-benzothiadiazole) has received significant interest because of its exceptional hole mobility despite near-amorphous thin-film morphology and brittleness at low Mn. In comparison, poly(indacenodithiophene-benzopyrollodione) (PIDTBPD) a lower but is exceptionally ductile similar Herein, we synthesize random indacenodithiophene (IDT) copolymers with varying amounts incorporated benzothiadiazole benzopyrollodione (BPD), which introduces varied degrees backbone twist to...

10.1021/acs.macromol.0c00512 article EN Macromolecules 2020-08-18

Green chemistry and a natural product together provide cost-effective, safe scalable solution to create luminophores with suppressed aggregation quenching in organic semiconductors.

10.1039/c9gc03391b article EN Green Chemistry 2019-01-01

Transmuting a natural product in chocolate into phosphors for light-emitting diodes.

10.1039/d1tc01567b article EN Journal of Materials Chemistry C 2021-01-01

Abstract A comparative study involving bimetallic nickel catalysts designed from disubstituted N,N,N′,N′ ‐tetra(diphenylphosphanylmethyl)benzene diamine bridging ligands is reported. Catalyst behavior explored in the Kumada catalyst‐transfer polymerization (KCTP) using poly(3‐hexylthiophene) (P3HT) as model system. The success of a controlled monitored by analyzing monomer conversion, degree polymerization, end‐group identity, and molecular weight distribution. characterization P3HT obtained...

10.1002/macp.201900363 article EN Macromolecular Chemistry and Physics 2019-11-28

A strained, cyclic hydrocarbon comprising a meta ‐quaterphenyl‐based arc that is clamped by an alkyne tether was synthesized via Yamamoto coupling of dichloro precursor. DFT calculations (B3LYP/6‐31G*) indicate the lowest‐energy ground state adopts twisted, C 2 conformation bears 19.0 kcal/mol strain energy. X‐ray crystallographic analysis confirms that, in solid state, molecule twisted structure similar to calculated conformation. Exposure ortho ‐linked precursor conditions generates...

10.1002/ejoc.201900688 article EN European Journal of Organic Chemistry 2019-07-12

The Cover Feature shows a young archer carefully aiming his bow at target in the background. synthetic shown foreground incorporates short alkyne linker that clamps meta-quaterphenyl group, generating strain much like taut string creates tension an archer's bow. To illustrate this effect, cartoon threads through exterior benzene rings of quaterphenyl unit and tightens knot, drawing benzenes closer together. Photograph courtesy Alan Richard. More information can be found Full Paper by D. K....

10.1002/ejoc.201900998 article EN European Journal of Organic Chemistry 2019-07-18
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