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21دورية أكاديمية
المؤلفون: Duda, Eimantas, Madayanad Suresh, Subeesh, Hall, David, Bagnich, Sergey, Saxena, Rishabh, Cordes, David B., Slawin, Alexandra M. Z., Beljonne, David, Olivier, Yoann, Köhler, Anna, Zysman-Colman, Eli
المساهمون: The Leverhulme Trust, The Royal Society, European Commission, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Centre for Energy Ethics
مصطلحات موضوعية: QD Chemistry, DAS, MCC, QD
وصف الملف: application/pdf
العلاقة: Chemistry of Materials; 283382964; f8986f41-e3e9-4526-83b0-2cfdafa123d8; 85149101948; Duda , E , Madayanad Suresh , S , Hall , D , Bagnich , S , Saxena , R , Cordes , D B , Slawin , A M Z , Beljonne , D , Olivier , Y , Köhler , A & Zysman-Colman , E 2023 , ' An oligomer approach for blue thermally activated delayed fluorescent emitters based on twisted donor-acceptor units ' , Chemistry of Materials , vol. 35 , no. 5 , pp. 2027-2037 . https://doi.org/10.1021/acs.chemmater.2c03438Test; ORCID: /0000-0002-9527-6418/work/130204089; ORCID: /0000-0002-5366-9168/work/130204228; ORCID: /0000-0001-7183-6022/work/130204656; https://hdl.handle.net/10023/27099Test; https://doi.org/10.26434/chemrxiv-2022-sgszvTest; RPG-2016-047; SRF\R1\201089; 812872; 838885
الإتاحة: https://doi.org/10.1021/acs.chemmater.2c03438Test
https://doi.org/10.26434/chemrxiv-2022-sgszvTest
https://hdl.handle.net/10023/27099Test -
22دورية أكاديمية
المؤلفون: Siddique, Zumaira, Payne, Julia L., Sajjad, Muhammad Tariq, Mica, Natalie, Cordes, David B., Slawin, Alexandra M. Z., Samuel, Ifor D. W., Iqbal, Azhar, Irvine, John T. S.
المساهمون: EPSRC, University of St Andrews. EaSTCHEM, University of St Andrews. School of Chemistry, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. Organic Semiconductor Centre, University of St Andrews. School of Physics and Astronomy, University of St Andrews. Centre for Biophotonics, University of St Andrews. Condensed Matter Physics, University of St Andrews. Centre for Energy Ethics, University of St Andrews. Centre for Designer Quantum Materials
مصطلحات موضوعية: QD Chemistry, DAS, SDG 7 - Affordable and Clean Energy, AC, MCC, QD
وصف الملف: application/pdf
العلاقة: Journal of Materials Chemistry C; 282630499; f98407ff-5208-48c5-9dfe-4ceb50c5d985; 85144710390; 000901704800001; Siddique , Z , Payne , J L , Sajjad , M T , Mica , N , Cordes , D B , Slawin , A M Z , Samuel , I D W , Iqbal , A & Irvine , J T S 2023 , ' Synthesis and optical characterization of lead-free phenylenediammonium bismuth halide perovskites : a long charge carrier lifetime in phenylenediammonium bismuth iodide ' , Journal of Materials Chemistry C , vol. 11 , no. 1 , pp. 223-234 . https://doi.org/10.1039/d2tc02601eTest; Jisc: 794784; ORCID: /0000-0002-8394-3359/work/125302993; ORCID: /0000-0002-9527-6418/work/125303132; ORCID: /0000-0002-5366-9168/work/125303173; ORCID: /0000-0003-3324-6018/work/125303192; https://hdl.handle.net/10023/28843Test; EP/P007821/1
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23دورية أكاديمية
المؤلفون: Matulaitis, Tomas, dos Santos, Paloma L, Tsuchiya, Youichi, Cordes, David B., Slawin, Alexandra M. Z., Adachi, Chihaya, Samuel, Ifor D. W., Zysman-Colman, Eli
المساهمون: EPSRC, University of St Andrews. Institute of Behavioural and Neural Sciences, 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, University of St Andrews. Centre for Energy Ethics
مصطلحات موضوعية: Bipolar, Charge transfer, DFT, Photophysics, Weak acceptor, QD Chemistry, DAS, MCC, QD
وصف الملف: application/pdf
العلاقة: ChemistrySelect; 283306476; 3e451fc2-15f5-4e41-ab68-c00e6637bbbf; 85150184388; Matulaitis , T , dos Santos , P L , Tsuchiya , Y , Cordes , D B , Slawin , A M Z , Adachi , C , Samuel , I D W & Zysman-Colman , E 2023 , ' Donor influence on the optoelectronic properties of N-substituted tetraphenylimidazole derivatives ' , ChemistrySelect , vol. 8 , no. 9 , e202300274 . https://doi.org/10.1002/slct.202300274Test; ORCID: /0000-0003-0470-7356/work/130203724; ORCID: /0000-0002-9527-6418/work/130204088; ORCID: /0000-0002-5366-9168/work/130204227; ORCID: /0000-0001-7183-6022/work/130204655; https://hdl.handle.net/10023/27083Test; EP/P010482/1; EP/R035164/1; ep/l017008/1
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24دورية أكاديمية
المؤلفون: Chalmers, Brian A., Cordes, David B., Bertram, Lauren, Harraghy, Daniel J., Reid, Rachel C., Smellie, Iain A., Tarcza, Anna E., Thomson, Brodie J.
المساهمون: University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM
مصطلحات موضوعية: X-ray crystallography, Bimetallic complexes, UV-vis spectroscopy, HRMS spectrometry, QD Chemistry, DAS, MCC, QD
وصف الملف: application/pdf
العلاقة: Molbank; 283227581; 1a3b1aac-33f3-4f4c-90ff-24cc3d636e2e; 85152285496; Chalmers , B A , Cordes , D B , Bertram , L , Harraghy , D J , Reid , R C , Smellie , I A , Tarcza , A E & Thomson , B J 2023 , ' Heteronuclear bimetallic complexes with 3 d and 4 f elements ' , Molbank , vol. 2023 , no. 1 , M1577 . https://doi.org/10.3390/M1577Test; RIS: urn:F54F853AABA2A53BBC87FEB42CFFCA89; ORCID: /0000-0002-2999-2272/work/128096957; ORCID: /0000-0002-5366-9168/work/128097430; ORCID: /0000-0002-5829-6487/work/128097638; https://hdl.handle.net/10023/26901Test
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25دورية أكاديمية
المؤلفون: Yuan, Ding, Goodfellow, Alister S., Duan, Zhuan, Kang, Tengfei, Kasten, Kevin, Cordes, David B., McKay, Aidan, Buehl, Michael, Boyce, Gregory R., Smith, Andrew D.
المساهمون: EPSRC, UK Research and Innovation, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM
مصطلحات موضوعية: QD Chemistry, DAS, QD
وصف الملف: application/pdf
العلاقة: Chemical Science; 296736644; 936ccee5-dc90-4ebc-b4a7-f1f78f61acc0; 85179152614; Yuan , D , Goodfellow , A S , Duan , Z , Kang , T , Kasten , K , Cordes , D B , McKay , A , Buehl , M , Boyce , G R & Smith , A D 2023 , ' Understanding divergent substrate stereoselectivity in the isothiourea-catalysed conjugate addition of cyclic α-substituted β-ketoesters to α,β-unsaturated aryl esters ' , Chemical Science , vol. 14 , no. 48 , pp. 14146-14156 . https://doi.org/10.1039/D3SC05470ETest; ORCID: /0000-0002-1095-7143/work/147967096; ORCID: /0000-0002-5366-9168/work/147967115; ORCID: /0000-0002-2104-7313/work/147967336; https://hdl.handle.net/10023/28822Test; EP/T023643/1; EP/W007517/1
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26دورية أكاديمية
المؤلفون: Demidov, Nikita, Grebogi, Mateus, Bourne, Connor, McKay, Aidan, Cordes, David B., Stasch, Andreas
المساهمون: University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM
مصطلحات موضوعية: Aniline synthesis, Azides, β-diketiminates, Magnesium hydride, Metal-halogen exchange, Organolithium reagents, Sterically demanding N-ligands, Terphenyl ligands, Triazenes, QD Chemistry, DAS, QD
وصف الملف: application/pdf
العلاقة: Molecules; 296042247; 639660af-d5ae-412f-8dc1-b5a1ec6b1b54; 85177776013; Demidov , N , Grebogi , M , Bourne , C , McKay , A , Cordes , D B & Stasch , A 2023 , ' A convenient one-pot synthesis of a sterically demanding aniline from aryllithium using trimethylsilyl azide, conversion to β -diketimines and synthesis of a β -diketiminate magnesium hydride complex ' , Molecules , vol. 28 , no. 22 , 7569 . https://doi.org/10.3390/molecules28227569Test; ORCID: /0000-0002-5366-9168/work/146963929; ORCID: /0000-0002-7407-8287/work/146965227; https://hdl.handle.net/10023/28685Test; https://www.mdpi.com/1420-3049/28/22/7569Test; https://www.mdpi.com/journal/molecules/special_issues/BLQABNA176Test
الإتاحة: https://doi.org/10.3390/molecules28227569Test
https://hdl.handle.net/10023/28685Test
https://www.mdpi.com/1420-3049/28/22/7569Test
https://www.mdpi.com/journal/molecules/special_issues/BLQABNA176Test -
27دورية أكاديمية
المؤلفون: Liu, Hang, Hafeez, Hassan, Cordes, David B., Slawin, Alexandra M. Z., Peters, Gavin, Lee, Steve, Samuel, Ifor D. W., Morrison, Finlay D.
المساهمون: EPSRC, University of St Andrews. EaSTCHEM, University of St Andrews. School of Chemistry, University of St Andrews. Centre for Designer Quantum Materials, University of St Andrews. Condensed Matter Physics, University of St Andrews. School of Physics and Astronomy, University of St Andrews. Centre for Biophotonics
مصطلحات موضوعية: QD Chemistry, DAS, MCC, QD
وصف الملف: application/pdf
العلاقة: Inorganic Chemistry; 283165980; b72affde-389a-43dd-a391-1f7087225431; 85148364047; Liu , H , Hafeez , H , Cordes , D B , Slawin , A M Z , Peters , G , Lee , S , Samuel , I D W & Morrison , F D 2023 , ' Enhanced photoluminescence and reduced dimensionality via vacancy ordering in a 10H halide perovskite ' , Inorganic Chemistry , vol. 62 , no. 8 , pp. 3629-3636 . https://doi.org/10.1021/acs.inorgchem.2c04433Test; ORCID: /0000-0002-9527-6418/work/129147256; ORCID: /0000-0002-5366-9168/work/129147713; ORCID: /0000-0002-2813-3142/work/129147783; ORCID: /0000-0002-2020-3310/work/129148090; https://hdl.handle.net/10023/26977Test; EP/R023751/1; EP/T019298/1
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28دورية أكاديمية
المؤلفون: Chen, Dongyang, Zhang, Le, Matulaitis, Tomas, Cordes, David B., Slawin, Alexandra M. Z., Zhang, Xiao-Hong, Samuel, Ifor D. W., Zysman-Colman, Eli
المساهمون: EPSRC, The Royal Society, University of St Andrews. EaSTCHEM, 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. Institute of Behavioural and Neural Sciences, University of St Andrews. Centre for Biophotonics, University of St Andrews. Condensed Matter Physics, University of St Andrews. Centre for Energy Ethics
مصطلحات موضوعية: QD Chemistry, DAS, QD
وصف الملف: application/pdf
العلاقة: Journal of Materials Chemistry C; 293904172; 3edeeb5c-d457-4d1f-97a0-f36ede910188; 85172273776; Chen , D , Zhang , L , Matulaitis , T , Cordes , D B , Slawin , A M Z , Zhang , X-H , Samuel , I D W & Zysman-Colman , E 2023 , ' Tuning the emission and exciton utilization mechanisms of pyrazine-based multi-carbazole emitters and their use in organic light-emitting diodes ' , Journal of Materials Chemistry C , vol. 11 , no. 38 , pp. 13095-13105 . https://doi.org/10.1039/d3tc02463fTest; Jisc: 1338241; publisher-id: d3tc02463f; ORCID: /0000-0003-0470-7356/work/142498951; ORCID: /0000-0002-9527-6418/work/142499220; ORCID: /0000-0002-5366-9168/work/142499308; ORCID: /0000-0001-7183-6022/work/142499563; https://hdl.handle.net/10023/28404Test; EP/P010482/1; ep/l017008/1; SRF\R1\201089
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29دورية أكاديمية
المؤلفون: Aitken, R Alan, Cordes, David B., McKay, Aidan, Sonecha, Dheirya K.
المساهمون: University of St Andrews. EaSTCHEM, University of St Andrews. School of Chemistry
مصطلحات موضوعية: X-ray structure, Hydrogen bonding, N-acylhydroxylamines, QD Chemistry, DAS, QD
وصف الملف: application/pdf
العلاقة: Molbank; 293817713; 81e221ab-bfe1-446d-83a3-013156f08615; 85172760675; Aitken , R A , Cordes , D B , McKay , A & Sonecha , D K 2023 , ' tert -Butyl N -hydroxycarbamate ( N -Boc-hydroxylamine) ' , Molbank , vol. 2023 , no. 3 , M1728 . https://doi.org/10.3390/M1728Test; ORCID: /0000-0001-6959-5311/work/142904655; ORCID: /0000-0002-5366-9168/work/142905043; https://hdl.handle.net/10023/28413Test; https://www.mdpi.com/1422-8599/2023/3/M1728Test
الإتاحة: https://doi.org/10.3390/M1728Test
https://hdl.handle.net/10023/28413Test
https://www.mdpi.com/1422-8599/2023/3/M1728Test -
30دورية أكاديمية
المساهمون: University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. Biomedical Sciences Research Complex
مصطلحات موضوعية: Electrostatic gauche effect, Calimimetics, Cinacalcet, Fluorinated drugs, Calcium receptors, Asymmetric fluorination, QD Chemistry, RR-NDAS, MCC, QD
وصف الملف: application/pdf
العلاقة: Medicinal Chemistry Research; 290321372; 3d84c7c3-7974-4be2-92ce-c094e89a2c5f; 85165515055; Renault , Y J G , Diao , J , Cordes , D B , Leach , K & O'Hagan , D 2023 , ' Direct syntheses of stereoisomers of 3-fluoro GABA and β-fluoroamine analogues of the calcium receptor (CaR) agonists, cinacalcet, tecalcet, fendilines and NPS R-467 ' , Medicinal Chemistry Research , vol. 32 , pp. 1532-1542 . https://doi.org/10.1007/s00044-023-03103-0Test; ORCID: /0000-0002-0510-5552/work/139552080; ORCID: /0000-0002-5366-9168/work/139554074; https://hdl.handle.net/10023/28018Test