المؤلفون: Wu, Sen, Gupta, Abhishek Kumar, Yoshida, Kou, Gong, Junyi, Hall, David, Cordes, David B., Slawin, Alexandra M. Z., Samuel, Ifor D. W., Zysman-Colman, Eli

المساهمون: The Royal Society, EPSRC, The Leverhulme Trust, University of St Andrews. School of Chemistry, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. School of Physics and Astronomy, University of St Andrews. EaSTCHEM, University of St Andrews. Centre for Biophotonics, University of St Andrews. Condensed Matter Physics, University of St Andrews. Centre for Energy Ethics

مصطلحات موضوعية: Multi-resonant thermally activated delayed fluorescence, Organic light-emitting diodes, Horizontal orientation, Hyperfluorescence, Thermally activated delayed fluorescence (TADF), QD Chemistry, DAS, MCC, QD

وصف الملف: application/pdf

العلاقة: Angewandte Chemie International Edition; 281895677; 5c441a69-89a7-4988-bf7e-537cbafd28c9; 85143229733; 000888992100001; Wu , S , Gupta , A K , Yoshida , K , Gong , J , Hall , D , Cordes , D B , Slawin , A M Z , Samuel , I D W & Zysman-Colman , E 2022 , ' Highly efficient green and red narrowband emissive organic light-emitting diodes employing multi-resonant thermally activated delayed fluorescence emitters ' , Angewandte Chemie International Edition , vol. 61 , no. 52 , e202213697 . https://doi.org/10.1002/anie.202213697Test; RIS: urn:F67ED02A79F46AF7D8EBB29946B8E3CA; ORCID: /0000-0002-9527-6418/work/123614043; ORCID: /0000-0002-5366-9168/work/123614171; ORCID: /0000-0002-9995-6525/work/123614380; ORCID: /0000-0001-7183-6022/work/123614574; https://hdl.handle.net/10023/26482Test; https://doi.org/10.26434/chemrxiv-2022-1j3np-v2Test; NF171163; ep/l017008/1; EP/P010482/1; SRF\R1\201089; RPG-2016-047

الإتاحة: https://doi.org/10.1002/anie.202213697Test
https://doi.org/10.26434/chemrxiv-2022-1j3np-v2Test
https://hdl.handle.net/10023/26482Test

المؤلفون: Main, Russell Matthew, Cordes, David B., Desai, Aamod V., Slawin, Alexandra M. Z., Wheatley, Paul, Armstrong, A. Robert, Morris, Russell E.

المساهمون: European Research Council, The Faraday Institution, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM

مصطلحات موضوعية: scXRD, VTXRD, TK, Electrochemistry, BioMOF, DAS, QD, Calcium MOF, QD Chemistry, MOF, TK Electrical engineering. Electronics Nuclear engineering

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_______901::910c4b493d9dd012986cd51d3d020b40Test
https://hdl.handle.net/10023/24381Test

المؤلفون: Henwood, Adam F., Bansal, Ashu K., Cordes, David B., Slawin, Alexandra M. Z., Samuel, Ifor D. W., Zysman-Colman, Eli

المساهمون: EPSRC, University of St Andrews. School of Chemistry, University of St Andrews. Organic Semiconductor Centre, University of St Andrews. School of Physics and Astronomy, University of St Andrews. EaSTCHEM, University of St Andrews. Condensed Matter Physics

مصطلحات موضوعية: QD Chemistry, NDAS, BDC, QD

وصف الملف: application/pdf

العلاقة: Journal of Materials Chemistry C; Henwood , A F , Bansal , A K , Cordes , D B , Slawin , A M Z , Samuel , I D W & Zysman-Colman , E 2016 , ' Solubilised bright blue-emitting iridium complexes for solution processed OLEDs ' , Journal of Materials Chemistry C , vol. 4 , no. 17 , pp. 3726-3737 . https://doi.org/10.1039/C6TC00151CTest; PURE: 240792034; PURE UUID: 232c436a-e654-4a8d-825e-31541db71216; Scopus: 84966364910; ORCID: /0000-0002-5366-9168/work/28023981; ORCID: /0000-0001-7183-6022/work/56639089; ORCID: /0000-0002-9527-6418/work/56861692; WOS: 000375697000008; http://hdl.handle.net/10023/8200Test; https://doi.org/10.1039/C6TC00151CTest; http://www.rsc.org/suppdata/c6/tc/c6tc00151c/c6tc00151c1.pdfTest; http://www.rsc.org/suppdata/c6/tc/c6tc00151c/c6tc00151c2.cifTest; EP/M02105X/1; EP/J01771X/1

الإتاحة: https://doi.org/10.1039/C6TC00151CTest
http://hdl.handle.net/10023/8200Test
http://www.rsc.org/suppdata/c6/tc/c6tc00151c/c6tc00151c1.pdfTest
http://www.rsc.org/suppdata/c6/tc/c6tc00151c/c6tc00151c2.cifTest

المؤلفون: Clark, Joshua, Neyyappadath, Rifahath M., Yu, Cihang, Slawin, Alexandra M. Z., Cordes, David B., O'Hagan, David

المساهمون: EPSRC, University of St Andrews. School of Chemistry, University of St Andrews. Biomedical Sciences Research Complex, University of St Andrews. EaSTCHEM

مصطلحات موضوعية: Organofluorine chemistry, Janus motif, Aryl hydrogenation, Organic chemistry, Fluorocyclohexanes, QD Chemistry, QH301 Biology, R Medicine, DAS, QD, QH301

وصف الملف: application/pdf

العلاقة: Chemistry - A European Journal; 275759219; 3eb00041-ec0a-4aa9-823b-4397ad369478; 85116415558; 000703997000001; Clark , J , Neyyappadath , R M , Yu , C , Slawin , A M Z , Cordes , D B & O'Hagan , D 2021 , ' Janus all- cis 2,3,4,5,6-pentafluorocyclohexyl building blocks applied to medicinal chemistry and bioactives discovery chemistry ' , Chemistry - A European Journal , vol. 27 , no. 64 , 202102819 , pp. 16000-16005 . https://doi.org/10.1002/chem.202102819Test; RIS: urn:222867F1684BC4E4C2572CF96C419D0D; ORCID: /0000-0002-0510-5552/work/101217835; ORCID: /0000-0002-9527-6418/work/101217853; ORCID: /0000-0002-5366-9168/work/101217884; https://hdl.handle.net/10023/24093Test; EP/R013799/1; EP/L016419/1

الإتاحة: https://doi.org/10.1002/chem.202102819Test
https://hdl.handle.net/10023/24093Test

المؤلفون: McGeachie, Liam J. R., Buehl, Michael, Cordes, David B., Slawin, Alexandra Martha Zoya, Woollins, J Derek

المساهمون: University of St Andrews. EaSTCHEM, University of St Andrews. School of Chemistry

مصطلحات موضوعية: QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: Inorganic Chemistry; 274090382; 290a37e4-37f2-4b5f-b09b-db47dad6635c; 000664576700010; 85108365043; McGeachie , L J R , Buehl , M , Cordes , D B , Slawin , A M Z & Woollins , J D 2021 , ' Bridging (thionylimido)metal complexes ' , Inorganic Chemistry , vol. Articles ASAP . https://doi.org/10.1021/acs.inorgchem.1c00725Test; ORCID: /0000-0002-1095-7143/work/95041726; ORCID: /0000-0002-9527-6418/work/95041871; ORCID: /0000-0002-1498-9652/work/95041876; ORCID: /0000-0002-5366-9168/work/95041879; https://hdl.handle.net/10023/23285Test

الإتاحة: https://doi.org/10.1021/acs.inorgchem.1c00725Test
https://hdl.handle.net/10023/23285Test

المؤلفون: Bell, Nicola, Xu, Chao, Fyfe, Jamie, Vantourout , Julien C., Brals, Jeremy, Chabbra, Sonia, Bode, Bela E., Cordes, David B., Slawin, Alexandra M. Z., McGuire, Thomas M., Watson, Allan J. B.

المساهمون: The Leverhulme Trust, EPSRC, University of St Andrews. Sir James Mackenzie Institute for Early Diagnosis, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex, University of St Andrews. Centre of Magnetic Resonance

مصطلحات موضوعية: Arylation, Boron, Copper, Cross-coupling, Mechanism, QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: Angewandte Chemie International Edition; 272350142; 172ab71c-27a4-40ca-b425-aec8626bcb34; 85101660531; 000621803100001; Bell , N , Xu , C , Fyfe , J , Vantourout , J C , Brals , J , Chabbra , S , Bode , B E , Cordes , D B , Slawin , A M Z , McGuire , T M & Watson , A J B 2021 , ' Cu(OTf) 2 -mediated cross-coupling of nitriles and N-heterocycles with arylboronic acids to generate nitrilium and pyridinium products ' , Angewandte Chemie International Edition , vol. 60 , no. 14 , pp. 7935-7940 . https://doi.org/10.1002/anie.202016811Test; ORCID: /0000-0002-9527-6418/work/89627884; ORCID: /0000-0002-5366-9168/work/89627962; ORCID: /0000-0002-3384-271X/work/89628055; ORCID: /0000-0002-1582-4286/work/89628279; https://hdl.handle.net/10023/21513Test; RPG-2015-308; EP/R025754/1

الإتاحة: https://doi.org/10.1002/anie.202016811Test
https://hdl.handle.net/10023/21513Test

المؤلفون: Nagar, Suryakant, Chatterjee, Sucheta, Goswami, Dibakar, Cordes, David B., Slawin, A.M.Z., Chauhan, Rohit Singh, Prabhu, Pradnya

المساهمون: University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM

مصطلحات موضوعية: QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: Inorganica Chimica Acta; Nagar , S , Chatterjee , S , Goswami , D , Cordes , D B , Slawin , A M Z , Chauhan , R S & Prabhu , P 2020 , ' Reactivity of nickel metal precursors towards amido linked N -heterocyclic carbenes and their catalytic studies for cross coupling reactions ' , Inorganica Chimica Acta , vol. 504 , 119446 . https://doi.org/10.1016/j.ica.2020.119446Test; PURE: 266096985; PURE UUID: a90eb134-a002-4fdf-8e0d-121effd8da45; RIS: urn:18585AEEACB52FD95796334C85C76B38; ORCID: /0000-0002-9527-6418/work/68281331; ORCID: /0000-0002-5366-9168/work/68281388; Scopus: 85078149280; WOS: 000514816900017; http://hdl.handle.net/10023/21278Test; https://doi.org/10.1016/j.ica.2020.119446Test

الإتاحة: https://doi.org/10.1016/j.ica.2020.119446Test
http://hdl.handle.net/10023/21278Test

المؤلفون: Gupta, Abhishek Kumar, Matulaitis, Tomas, Cordes, David B., Slawin, Alexandra M. Z., Samuel, Ifor D. W., Zysman-Colman, Eli

المساهمون: Scottish Funding Council, The Royal Society, EPSRC, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Centre for Biophotonics, University of St Andrews. Condensed Matter Physics, University of St Andrews. School of Physics and Astronomy

مصطلحات موضوعية: TADF, OLEDs, α-diketone, Red-shift emission, QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: Canadian Journal of Chemistry; 275956900; 6ac445f9-e39b-4597-b06d-5b2c9c3d8949; 000767175100008; 85125885942; Gupta , A K , Matulaitis , T , Cordes , D B , Slawin , A M Z , Samuel , I D W & Zysman-Colman , E 2021 , ' Highly twisted α-diketone-based thermally activated delayed fluorescence emitters and their use in organic light-emitting diodes ' , Canadian Journal of Chemistry , vol. Early View . https://doi.org/10.1139/cjc-2021-0208Test; ORCID: /0000-0002-9527-6418/work/100901067; ORCID: /0000-0002-5366-9168/work/100901103; ORCID: /0000-0001-7183-6022/work/100901526; ORCID: /0000-0003-0470-7356/work/100901633; https://hdl.handle.net/10023/24060Test; N/A; NF171163; EP/P010482/1; ep/l017008/1

الإتاحة: https://doi.org/10.1139/cjc-2021-0208Test
https://hdl.handle.net/10023/24060Test

المؤلفون: Al-Maharik, Nawaf, Cordes, David B., Slawin, Alexandra M. Z., Buhl, Michael, O'Hagan, David

المساهمون: University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

مصطلحات موضوعية: Bond-forming reactions, 3 vicinal fluorines, In-situ generation, Organofluorine chemistry, Aldehydes, Reagents, Motifs, QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: Organic & Biomolecular Chemistry; 266558751; d3d5d7ef-83ac-4a07-8980-ca286f4fbad5; 000512061200009; 85079023177; Al-Maharik , N , Cordes , D B , Slawin , A M Z , Buhl , M & O'Hagan , D 2020 , ' Probing the helical integrity of multivicinal all- syn -fluoro alkanes ' , Organic & Biomolecular Chemistry , vol. 18 , no. 5 , pp. 878-887 . https://doi.org/10.1039/c9ob02647aTest; ORCID: /0000-0002-1095-7143/work/69834806; ORCID: /0000-0002-0510-5552/work/69834813; ORCID: /0000-0002-9527-6418/work/69834851; ORCID: /0000-0002-5366-9168/work/69834895; https://hdl.handle.net/10023/21231Test

الإتاحة: https://doi.org/10.1039/c9ob02647aTest
https://hdl.handle.net/10023/21231Test

المؤلفون: Hayes, Oliver G, Warrender, Stewart James, Cordes, David B., Duncan, Morven J., Slawin, Alexandra M. Z., Morris, Russell E.

المساهمون: EPSRC, European Commission, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM

مصطلحات موضوعية: Crystalline-crystalline transformation, Doping, Metal-organic frameworks, Nitric oxide, Structure elucidation, QD Chemistry, DAS, QD

وصف الملف: application/pdf

العلاقة: European Journal of Inorganic Chemistry; 267778109; abe68e3c-abd7-4cf4-bb62-8c46405f5f70; 85085569353; 000535628900001; Hayes , O G , Warrender , S J , Cordes , D B , Duncan , M J , Slawin , A M Z & Morris , R E 2020 , ' Preventing undesirable structure flexibility in pyromellitate metal organic frameworks ' , European Journal of Inorganic Chemistry , vol. 2020 , no. 26 , pp. 2537-2544 . https://doi.org/10.1002/ejic.202000322Test; ORCID: /0000-0002-9527-6418/work/74872893; ORCID: /0000-0002-5366-9168/work/74872966; ORCID: /0000-0001-7809-0315/work/74872969; https://hdl.handle.net/10023/20005Test; EP/K005499/1; EP/K039210/1; 685727

الإتاحة: https://doi.org/10.1002/ejic.202000322Test
https://hdl.handle.net/10023/20005Test