D. Crossley

发表

Synthesis and photochromic properties of spiro[naphthopyran-7′H- benzocyclohepta-5′,8′-dienes]

C. D. Gabbutt, B. M. Heron, Martin Mogstad, 2012 .

Facile Arylation of Four-Coordinate Boron Halides by Borenium Cation Mediated Boro-desilylation and -destannylation

M. Turner, M. Ingleson, J. Cid, 2015, Organometallics.

2,2,4,6-Tetraaryl-2H-benzo[h]chromenes: The influence of electronic communication between aryl substituents on their photochromism

D. Jacquemin, C. D. Gabbutt, B. M. Heron, 2021, Dyes and Pigments.

Enhancing electron affinity and tuning band gap in donor–acceptor organic semiconductors by benzothiadiazole directed C–H borylation

M. Turner, I. Vitorica-Yrezabal, M. Ingleson, 2015, Chemical science.

Benzoselenadiazole and benzotriazole directed electrophilic C–H borylation of conjugated donor–acceptor materials

Daniel J. Tate, M. Turner, Ji‐Seon Kim, 2019, Journal of Materials Chemistry C.

Synthesis, Characterization, and Functionalization of 1‐Boraphenalenes

M. Ingleson, J. Cid, J. E. Radcliffe, 2018, Angewandte Chemie.

Borylated Arylamine–Benzothiadiazole Donor–Acceptor Materials as Low-LUMO, Low-Band-Gap Chromophores

M. Turner, I. Vitorica-Yrezabal, M. Ingleson, 2017 .

Highly Emissive Far Red/Near‐IR Fluorophores Based on Borylated Fluorene–Benzothiadiazole Donor–Acceptor Materials

M. Turner, M. Humphries, I. Vitorica-Yrezabal, 2016, Chemistry.

Post-polymerization C-H Borylation of Donor-Acceptor Materials Gives Highly Efficient Solid State Near-Infrared Emitters for Near-IR-OLEDs and Effective Biological Imaging.

M. Turner, M. Humphries, L. Dailey, 2017, ACS applied materials & interfaces.

Generation of a series of Bn fused oligo-naphthalenes (n = 1 to 3) from a B1-polycyclic aromatic hydrocarbon.

M. Ingleson, V. Fasano, G. Whitehead, 2018, Chemical communications.

A modular route to boron doped PAHs by combining borylative cyclisation and electrophilic C–H borylation

I. Vitorica-Yrezabal, M. Ingleson, J. Cid, 2017, Chemical science.

Inter- and intra-molecular C-H borylation for the formation of PAHs containing triarylborane and indole units.

I. Vitorica-Yrezabal, M. Ingleson, I. Cade, 2016, Dalton transactions.

Dose intercomparison between BARC (India) and NPL (UK) using glutamine (spectrophotometric readout) and dichromate dosimeters

P. Sharpe, B. L. Gupta, D. Crossley, 1999 .

C−H Borylation/Cross‐Coupling Forms Twisted Donor–Acceptor Compounds Exhibiting Donor‐Dependent Delayed Emission

M. Turner, I. Vitorica-Yrezabal, M. Ingleson, 2018, Chemistry.

In vivo optical performance of a new class of near infrared-emitting conjugated polymers: borylated PF8-BT.

M. Turner, J. Rao, L. Dailey, 2019, ACS applied materials & interfaces.

C−H Borylation/Cross‐Coupling Forms Twisted Donor–Acceptor Compounds Exhibiting Donor‐Dependent Delayed Emission

M. Turner, I. Vitorica-Yrezabal, M. Ingleson, 2018, Chemistry.