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: Yu, Cihang, Kütt, Agnes, Röschenthaler, Gerd-Volker, Lebl, Tomas, Cordes, David B., Slawin, Alexandra M. Z., Buehl, 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: Janus face, Cyclohexanes, Trifluoromethyl groups, Aryl hydrogenation, Triaxial orientations, QD Chemistry, DAS, BDC, R2C, QD

وصف الملف: application/pdf

العلاقة: Angewandte Chemie International Edition; 269274158; b39e5a2e-7612-4c18-9963-dc8b3720bb9a; 85090058738; 000564434400001; Yu , C , Kütt , A , Röschenthaler , G-V , Lebl , T , Cordes , D B , Slawin , A M Z , Buehl , M & O'Hagan , D 2020 , ' Janus face all- cis 1,2,4,5-tetrakis(trifluoromethyl)- and all- cis 1,2,3,4,5,6-hexakis(trifluoromethyl)- cyclohexanes ' , Angewandte Chemie International Edition , vol. 59 , no. 45 , pp. 19905-19909 . https://doi.org/10.1002/anie.202008662Test; RIS: urn:E304C0A09AD8144559065E07F8A97B2F; ORCID: /0000-0002-0269-3221/work/79917784; ORCID: /0000-0002-1095-7143/work/79917822; ORCID: /0000-0002-0510-5552/work/79917827; ORCID: /0000-0002-9527-6418/work/79917833; ORCID: /0000-0002-5366-9168/work/79917848; https://hdl.handle.net/10023/20964Test

الإتاحة: https://doi.org/10.1002/anie.202008662Test
https://hdl.handle.net/10023/20964Test

المؤلفون: Tian, Jiyu, Cordes, David B., Quarti, Claudio, Beljonne, David, Slawin, Alexandra M. Z., Zysman-Colman, Eli, Morrison, Finlay D.

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

مصطلحات موضوعية: Perovskite, Organic-inorganic hybrid perovskite, Halide perovskite, Electronic structure, Density functional theory (DFT), Dielectric properties, QD Chemistry, DAS, BDC, SDG 7 - Affordable and Clean Energy, QD

وصف الملف: application/pdf

العلاقة: ACS Applied Energy Materials; 260459047; b6c465e8-3c35-4f8c-bb8b-e9280de33698; 85070616279; 000483434700012; Tian , J , Cordes , D B , Quarti , C , Beljonne , D , Slawin , A M Z , Zysman-Colman , E & Morrison , F D 2019 , ' Stable 6H organic-inorganic hybrid lead perovskite and competitive formation of 6H and 3C perovskite structure with mixed A cations ' , ACS Applied Energy Materials , vol. 2 , no. 8 , pp. 5427-54737 . https://doi.org/10.1021/acsaem.9b00419Test; ORCID: /0000-0002-2813-3142/work/60427075; ORCID: /0000-0002-9527-6418/work/60427079; ORCID: /0000-0002-5366-9168/work/60427156; ORCID: /0000-0001-7183-6022/work/60427619; https://hdl.handle.net/10023/20286Test

الإتاحة: https://doi.org/10.1021/acsaem.9b00419Test
https://hdl.handle.net/10023/20286Test

المؤلفون: Greenhalgh, Mark D., Smith, Samuel M., Walden, Daniel M., Taylor, James E., Brice, Zamira, Robinson, Emily R. T., Fallan, Charlene, Cordes, David B., Slawin, Alexandra M. Z., Richardson, H. Camille, Grove, Markas A., Cheong, Paul Ha-Yeon, Smith, Andrew D.

المساهمون: The Royal Society, European Commission, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

مصطلحات موضوعية: Acylation, Kinetic resolution, Lewis bases, Organocatalysis, Tertiary alcohols, QD Chemistry, DAS, BDC, R2C, QD

وصف الملف: application/pdf

العلاقة: Angewandte Chemie International Edition; 252045715; d1b5cdb2-e2b0-405b-b952-a05053a6d2c7; 85042110491; 000426759900035; Greenhalgh , M D , Smith , S M , Walden , D M , Taylor , J E , Brice , Z , Robinson , E R T , Fallan , C , Cordes , D B , Slawin , A M Z , Richardson , H C , Grove , M A , Cheong , P H-Y & Smith , A D 2018 , ' A C=O•••isothiouronium interaction dictates enantiodiscrimination in acylative kinetic resolution of tertiary heterocyclic alcohols ' , Angewandte Chemie International Edition , vol. 57 , no. 12 , pp. 3200-3206 . https://doi.org/10.1002/anie.201712456Test; ORCID: /0000-0002-2104-7313/work/42023858; ORCID: /0000-0002-5366-9168/work/42023872; ORCID: /0000-0002-9527-6418/work/56861440; https://hdl.handle.net/10023/17091Test; WM140071; N/A

الإتاحة: https://doi.org/10.1002/anie.201712456Test
https://hdl.handle.net/10023/17091Test

المؤلفون: Giannoulis, Angeliki, Ackermann, Katrin, Spindler, Philipp, Higgins, Catherine, Cordes, David B., Slawin, Alexandra M. Z., Prisner, Thomas F., Bode, Bela E.

المساهمون: European Commission, EPSRC, The Wellcome Trust, 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: QC Physics, QD Chemistry, DAS, BDC, QC, QD

وصف الملف: application/pdf

العلاقة: Physical Chemistry Chemical Physics; 252649836; 8dc176e0-c22f-446c-8223-de44e829a1ca; 85046375673; 000431821800058; Giannoulis , A , Ackermann , K , Spindler , P , Higgins , C , Cordes , D B , Slawin , A M Z , Prisner , T F & Bode , B E 2018 , ' Nitroxide-nitroxide and nitroxide-metal distance measurements in transition metal complexes with two or three paramagnetic centres give access to thermodynamic and kinetic stabilities ' , Physical Chemistry Chemical Physics , vol. 20 , no. 16 , pp. 11196-11205 . https://doi.org/10.1039/C8CP01611ATest; ORCID: /0000-0002-5366-9168/work/43149750; ORCID: /0000-0002-3384-271X/work/43149877; ORCID: /0000-0002-9527-6418/work/56861626; https://hdl.handle.net/10023/17398Test; EP/M024660/1; 099149/Z/12/Z

الإتاحة: https://doi.org/10.1039/C8CP01611ATest
https://hdl.handle.net/10023/17398Test

المؤلفون: Lawrence, Samuel, Ohlin, C. André, Cordes, David B., Slawin, Alexandra M. Z., Stasch, Andreas

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

مصطلحات موضوعية: QD Chemistry, DAS, BDC, QD

وصف الملف: application/pdf

العلاقة: Chemical Science; 261540400; 93f0db7c-994c-4dba-b0cc-d10b6efdd65c; 85075338385; 000499471800009; Lawrence , S , Ohlin , C A , Cordes , D B , Slawin , A M Z & Stasch , A 2019 , ' Hydrocarbon-soluble, hexaanionic fulleride complexes of magnesium ' , Chemical Science , vol. 10 , no. 46 , pp. 10755-10764 . https://doi.org/10.1039/C9SC03857DTest; ORCID: /0000-0002-9527-6418/work/63045015; ORCID: /0000-0002-5366-9168/work/63045179; ORCID: /0000-0002-7407-8287/work/63046168; https://hdl.handle.net/10023/18702Test

الإتاحة: https://doi.org/10.1039/C9SC03857DTest
https://hdl.handle.net/10023/18702Test

المؤلفون: Widegren, Magnus B., Harkness, Gavin J., Slawin, Alexandra M. Z., Cordes, David B., Clarke, Matthew L.

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

مصطلحات موضوعية: Enantioselective catalysis, Ester hydrogenation, Ferrocene, Manganese, Reduction, QD Chemistry, DAS, BDC, R2C, QD

وصف الملف: application/pdf

العلاقة: Angewandte Chemie International Edition; 251304734; 91758ad4-7b36-4824-a1df-d11a7711dbf2; 000400755800030; 85018631758; Widegren , M B , Harkness , G J , Slawin , A M Z , Cordes , D B & Clarke , M L 2017 , ' A highly active manganese catalyst for enantioselective ketone and ester hydrogenation ' , Angewandte Chemie International Edition , vol. 56 , no. 21 , pp. 5825-5828 . https://doi.org/10.1002/anie.201702406Test; ORCID: /0000-0002-5366-9168/work/37446795; ORCID: /0000-0002-9527-6418/work/56861556; ORCID: /0000-0002-2444-1244/work/59464609; https://hdl.handle.net/10023/19939Test; http://hdl.handle.net/10023/13175Test

الإتاحة: https://doi.org/10.1002/anie.201702406Test
https://hdl.handle.net/10023/19939Test
http://hdl.handle.net/10023/13175Test

المؤلفون: Taylor, Laurence J., Buehl, Michael, Chalmers, Brian A., Ray, Matthew J., Wawrzyniak, Piotr, Walton, John C., Cordes, David B., Slawin, Alexandra M. Z., Woollins, J. Derek, Kilian, Petr

المساهمون: University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Office of the Principal

مصطلحات موضوعية: QD Chemistry, DAS, BDC, R2C, QD

وصف الملف: application/pdf

العلاقة: Journal of the American Chemical Society; 251693563; 77ad715b-fd42-4840-9d33-22933baffc0d; 85038570545; 000419082100026; Taylor , L J , Buehl , M , Chalmers , B A , Ray , M J , Wawrzyniak , P , Walton , J C , Cordes , D B , Slawin , A M Z , Woollins , J D & Kilian , P 2017 , ' Dealkanative main group couplings across the peri-gap ' , Journal of the American Chemical Society , vol. 139 , no. 51 , pp. 18545-18551 . https://doi.org/10.1021/jacs.7b08682Test; ORCID: /0000-0002-1095-7143/work/48131749; ORCID: /0000-0002-5366-9168/work/39487833; ORCID: /0000-0002-2999-2272/work/55901228; ORCID: /0000-0003-2746-6276/work/56638710; ORCID: /0000-0002-9527-6418/work/56861557; ORCID: /0000-0001-6379-3026/work/58285399; ORCID: /0000-0002-1498-9652/work/59464673; https://hdl.handle.net/10023/16583Test

الإتاحة: https://doi.org/10.1021/jacs.7b08682Test
https://hdl.handle.net/10023/16583Test

المؤلفون: Bidal, Yannick D., Santoro, Orlando, Melaimi, Mohand, Cordes, David B., Slawin, Alexandra M. Z., Bertrand, Guy, Cazin, Catherine S. J.

المساهمون: The Royal Society, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM

مصطلحات موضوعية: Abnormal, CAAC, Carbene transfer, Copper, N-heterocyclic carbene, QD Chemistry, DAS, BDC, QD

وصف الملف: application/pdf

العلاقة: Chemistry - A European Journal; 243306894; 522ad7d2-57c0-473b-b4b7-71a90959cd4b; 84971401706; 000380271100050; Bidal , Y D , Santoro , O , Melaimi , M , Cordes , D B , Slawin , A M Z , Bertrand , G & Cazin , C S J 2016 , ' Generalization of the copper to late-transition-metal transmetallation to carbenes beyond N -heterocyclic carbenes ' , Chemistry - A European Journal , vol. 22 , no. 27 , pp. 9404-9409 . https://doi.org/10.1002/chem.201601254Test; Bibtex: urn:4a10a1ea389c1886afb3d12e87f8a95f; ORCID: /0000-0002-5366-9168/work/28023977; ORCID: /0000-0002-9527-6418/work/56861732; https://hdl.handle.net/10023/10880Test; UF100691

الإتاحة: https://doi.org/10.1002/chem.201601254Test
https://hdl.handle.net/10023/10880Test

المؤلفون: Lahive, Ciaran, Deuss, Peter J., Lancefield, Christopher Stuart, Sun, Zhuohua, Cordes, David B., Young, Claire M., Tran, Fanny, Slawin, Alexandra M. Z., de Vries, Johannes G., Kamer, Paul C. J., Westwood, Nicholas J., Barta, Katalin

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

مصطلحات موضوعية: QD Chemistry, DAS, BDC, R2C, SDG 7 - Affordable and Clean Energy, QD

وصف الملف: application/pdf

العلاقة: Journal of the American Chemical Society; Lahive , C , Deuss , P J , Lancefield , C S , Sun , Z , Cordes , D B , Young , C M , Tran , F , Slawin , A M Z , de Vries , J G , Kamer , P C J , Westwood , N J & Barta , K 2016 , ' Advanced model compounds for understanding acid-catalyzed lignin depolymerization : identification of renewable aromatics and a lignin-derived solvent ' , Journal of the American Chemical Society , vol. 138 , no. 28 , pp. 8900-8911 . https://doi.org/10.1021/jacs.6b04144Test; PURE: 243473248; PURE UUID: 0606af3b-9f6b-481c-9139-dbce8d573de3; Scopus: 84979204228; ORCID: /0000-0002-5366-9168/work/28023975; ORCID: /0000-0003-0630-0138/work/56424173; ORCID: /0000-0002-9527-6418/work/56861735; WOS: 000380295600038; http://hdl.handle.net/10023/11013Test; https://doi.org/10.1021/jacs.6b04144Test; EP/J018139/1; EP/K00445X/1; SUBICAT

الإتاحة: https://doi.org/10.1021/jacs.6b04144Test
http://hdl.handle.net/10023/11013Test