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[ d ]-Carbon-carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines

Chemical science (Cambridge), 2016-01, Vol.7 (7), p.4211-4219

2016

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Beyond Doping and Charge Balancing: How Polymer Acid Templates Impact the Properties of Conducting Polymer Complexes

The journal of physical chemistry letters, 2017-09, Vol.8 (18), p.4530-4539

2017

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Development of a Platform for Near-Infrared Photoredox Catalysis

ACS central science, 2020-11, Vol.6 (11), p.2053-2059

2020

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High Performance OTFTs Fabricated Using a Calamitic Liquid Crystalline Material of 2-(4-Dodecyl phenyl)[1]benzothieno[3,2-b][1]benzothiophene

Advanced electronic materials, 2016-09, Vol.2 (9), p.n/a

2016

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Red-Shifting Blue Light Photoredox Catalysis for Organic Synthesis: A Graphical Review

SynOpen (2017), 2023-02, Vol.7 (1), p.76-87

2023

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Eliminating Piezoresistivity in Flexible Conducting Polymers for Accurate Temperature Sensing under Dynamic Mechanical Deformations

Small (Weinheim an der Bergstrasse, Germany), 2016-06, Vol.12 (21), p.2832-2838

2016

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Contorted Hexabenzocoronenes with Extended Heterocyclic Moieties Improve Visible-Light Absorption and Performance in Organic Solar Cells

Chemistry of materials, 2016-01, Vol.28 (2), p.673-681

2016

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[d]-Carbon-carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropinesElectronic supplementary information (ESI) available: The detailed synthetic procedures, characterization, NMR spectra, UV-vis and emission of diazaphosphepine derivatives. GIXD images of MI-PO-C8 and Di-MI-PO. CCDC 1427664-1427668. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc00519e

2016-06

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[d]-Carbon–carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines† †Electronic supplementary information (ESI) available: The detailed synthetic procedures, characterization, NMR spectra, UV-vis and emission of diazaphosphepine derivatives. GIXD images of MI-PO-C8 and Di-MI-PO. CCDC 1427664–1427668. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc00519e

Chemical science (Cambridge), 2016-03, Vol.7 (7), p.4211-4219

2016

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Predicting Performance of Photochemical Transformations for Scaling Up in Different Platforms by Combining High-Throughput Experimentation with Computational Modeling

Organic process research & development, 2020-10, Vol.24 (10), p.2128-2138

2020

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Emerging reaction technologies in pharmaceutical development: Challenges and opportunities in electrochemistry, photochemistry, and biocatalysis

Chemical engineering research & design, 2023-04, Vol.192, p.622-637

2023

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Overcoming Photochemical Limitations in Metallaphotoredox Catalysis: Red-Light-Driven C–N Cross-Coupling

Journal of the American Chemical Society, 2022-12, Vol.144 (49), p.22409-22415

2022

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Postdeposition Processing Influences the Relative Contributions of Electronic and Ionic Seebeck Effects in the Thermoelectric Response of Conducting Polymers

Journal of physical chemistry. C, 2021-05, Vol.125 (22)

2021

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Humidity and Strain Rate Determine the Extent of Phase Shift in the Piezoresistive Response of PEDOT:PSS

ACS applied materials & interfaces, 2019-05, Vol.11 (18), p.16888-16895

2019

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Tuning the Magnitude and the Polarity of the Piezoresistive Response of Polyaniline through Structural Control

ACS applied materials & interfaces, 2017-04, Vol.9 (14), p.12766-12772

2017

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Postdeposition Processing Influences the Relative Contributions of Electronic and Ionic Seebeck Effects in the Thermoelectric Response of Conducting Polymers

Journal of physical chemistry. C, 2021-06, Vol.125 (22), p.12289-12296

2021

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Liquid Crystals: High Performance OTFTs Fabricated Using a Calamitic Liquid Crystalline Material of 2-(4-Dodecyl phenyl)[1]benzothieno[3,2-b][1]benzothiophene (Adv. Electron. Mater. 9/2016)

Advanced electronic materials, 2016-09, Vol.2 (9), p.n/a

2016

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Photochemistry in Pharmaceutical Development: A Survey of Strategies and Approaches to Industry-wide Implementation

Organic process research & development, 2024-04, Vol.28 (4), p.831-846

2024

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Ni/Photoredox-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Alkyl Pinacolboronates and (Hetero)Aryl Bromides

Organic letters, 2022-08, Vol.24 (31), p.5663-5668

2022

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P(III) vs P(V): A P(V) Reagent for Thiophosphoramidate Linkages and Application to an Asymmetric Synthesis of a Cyclic Dinucleotide STING Agonist

Journal of organic chemistry, 2022-02, Vol.87 (4), p.1934-1940

2022

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Increasing saturation: development of broadly applicable photocatalytic C sp2 –C sp3 cross-couplings of alkyl trifluoroborates and (hetero)aryl bromides for array synthesis

Reaction chemistry & engineering, 2021-09, Vol.6 (9), p.1666-1676

2021

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Tuning Morphology and Melting Temperature in Polyethylene Films by MAPLE

Macromolecules, 2018-01, Vol.51 (2), p.512-519

2018

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Increasing saturation: development of broadly applicable photocatalytic C-C cross-couplings of alkyl trifluoroborates and (hetero)aryl bromides for array synthesis

Reaction chemistry & engineering, 2021-08, Vol.6 (9), p.1666-1676

2021

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Increasing saturation: development of broadly applicable photocatalytic Csp2–Csp3 cross-couplings of alkyl trifluoroborates and (hetero)aryl bromides for array synthesis

Reaction chemistry & engineering, 2021-01, Vol.6 (9), p.1666-1676

2021

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Formation of Organic Alloys in Ternary-Blend Solar Cells with Two Acceptors Having Energy-Level Offsets Exceeding 0.4 eV

ACS energy letters, 2017-09, Vol.2 (9), p.2149-2156

2017

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[ d ]-Carbon-carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines

Beyond Doping and Charge Balancing: How Polymer Acid Templates Impact the Properties of Conducting Polymer Complexes

Development of a Platform for Near-Infrared Photoredox Catalysis

High Performance OTFTs Fabricated Using a Calamitic Liquid Crystalline Material of 2-(4-Dodecyl phenyl)[1]benzothieno[3,2-b][1]benzothiophene

Red-Shifting Blue Light Photoredox Catalysis for Organic Synthesis: A Graphical Review

Eliminating Piezoresistivity in Flexible Conducting Polymers for Accurate Temperature Sensing under Dynamic Mechanical Deformations

Contorted Hexabenzocoronenes with Extended Heterocyclic Moieties Improve Visible-Light Absorption and Performance in Organic Solar Cells

Predicting Performance of Photochemical Transformations for Scaling Up in Different Platforms by Combining High-Throughput Experimentation with Computational Modeling

Emerging reaction technologies in pharmaceutical development: Challenges and opportunities in electrochemistry, photochemistry, and biocatalysis

Overcoming Photochemical Limitations in Metallaphotoredox Catalysis: Red-Light-Driven C–N Cross-Coupling

Postdeposition Processing Influences the Relative Contributions of Electronic and Ionic Seebeck Effects in the Thermoelectric Response of Conducting Polymers

Humidity and Strain Rate Determine the Extent of Phase Shift in the Piezoresistive Response of PEDOT:PSS

Tuning the Magnitude and the Polarity of the Piezoresistive Response of Polyaniline through Structural Control

Postdeposition Processing Influences the Relative Contributions of Electronic and Ionic Seebeck Effects in the Thermoelectric Response of Conducting Polymers

Liquid Crystals: High Performance OTFTs Fabricated Using a Calamitic Liquid Crystalline Material of 2-(4-Dodecyl phenyl)[1]benzothieno[3,2-b][1]benzothiophene (Adv. Electron. Mater. 9/2016)

Photochemistry in Pharmaceutical Development: A Survey of Strategies and Approaches to Industry-wide Implementation

Ni/Photoredox-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Alkyl Pinacolboronates and (Hetero)Aryl Bromides

P(III) vs P(V): A P(V) Reagent for Thiophosphoramidate Linkages and Application to an Asymmetric Synthesis of a Cyclic Dinucleotide STING Agonist

Increasing saturation: development of broadly applicable photocatalytic C sp2 –C sp3 cross-couplings of alkyl trifluoroborates and (hetero)aryl bromides for array synthesis

Tuning Morphology and Melting Temperature in Polyethylene Films by MAPLE

Increasing saturation: development of broadly applicable photocatalytic C-C cross-couplings of alkyl trifluoroborates and (hetero)aryl bromides for array synthesis

Increasing saturation: development of broadly applicable photocatalytic Csp2–Csp3 cross-couplings of alkyl trifluoroborates and (hetero)aryl bromides for array synthesis

Formation of Organic Alloys in Ternary-Blend Solar Cells with Two Acceptors Having Energy-Level Offsets Exceeding 0.4 eV

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