| Year |
Citation |
Score |
| 2023 |
Caine JR, Choi H, Hojo R, Hudson ZM. Organic Photothermal Materials Obtained Using Thermally Activated Delayed Fluorescence Design Principles. Chemistry (Weinheim An Der Bergstrasse, Germany). e202302861. PMID 38015005 DOI: 10.1002/chem.202302861 |
0.319 |
|
| 2023 |
Gupta R, Wang Y, Darwish GH, Poisson J, Szwarczewski A, Kim S, Traaseth C, Hudson ZM, Algar WR. Semiconducting Polymer Dots Directly Stabilized with Serum Albumin: Preparation, Characterization, and Cellular Immunolabeling. Acs Applied Materials & Interfaces. PMID 37983537 DOI: 10.1021/acsami.3c13430 |
0.302 |
|
| 2023 |
Primrose WL, Mayder DM, Hojo R, Hudson ZM. Dibenzodipyridophenazines with Dendritic Electron Donors Exhibiting Deep-Red Emission and Thermally Activated Delayed Fluorescence. The Journal of Organic Chemistry. PMID 36920272 DOI: 10.1021/acs.joc.2c02774 |
0.317 |
|
| 2023 |
Xu P, Hojo R, Hudson ZM. Thermally Activated Delayed Fluorescence and Room-Temperature Phosphorescence in Materials with Imidazo-pyrazine-5,6-dicarbonitrile Acceptors. Chemistry (Weinheim An Der Bergstrasse, Germany). e202203585. PMID 36806222 DOI: 10.1002/chem.202203585 |
0.345 |
|
| 2022 |
Mayder DM, Christopherson CJ, Primrose WL, Lin AS, Hudson ZM. Polymer dots and glassy organic dots using dibenzodipyridophenazine dyes as water-dispersible TADF probes for cellular imaging. Journal of Materials Chemistry. B. 10: 6496-6506. PMID 35979840 DOI: 10.1039/d2tb01252a |
0.307 |
|
| 2022 |
Genin SN, Ryabinkin IG, Paisley NR, Whelan SO, Helander MG, Hudson ZM. Estimating Phosphorescent Emission Energies in Ir Complexes Using Large-Scale Quantum Computing Simulations. Angewandte Chemie (International Ed. in English). e202116175. PMID 35285999 DOI: 10.1002/anie.202116175 |
0.714 |
|
| 2021 |
Mayder DM, Tonge CM, Nguyen GD, Tran MV, Tom G, Darwish GH, Gupta R, Lix K, Kamal S, Algar WR, Burke SA, Hudson ZM. Polymer Dots with Enhanced Photostability, Quantum Yield, and Two-Photon Cross-Section using Structurally Constrained Deep-Blue Fluorophores. Journal of the American Chemical Society. PMID 34618454 DOI: 10.1021/jacs.1c06094 |
0.333 |
|
| 2021 |
Polgar AM, Hudson ZM. Thermally activated delayed fluorescence materials as organic photosensitizers. Chemical Communications (Cambridge, England). PMID 34569578 DOI: 10.1039/d1cc04593h |
0.305 |
|
| 2021 |
Christopherson CJ, Paisley NR, Xiao Z, Algar WR, Hudson ZM. Red-Emissive Cell-Penetrating Polymer Dots Exhibiting Thermally Activated Delayed Fluorescence for Cellular Imaging. Journal of the American Chemical Society. PMID 34382775 DOI: 10.1021/jacs.1c06290 |
0.772 |
|
| 2021 |
Poisson J, Polgar AM, Fromel M, Pester CW, Hudson ZM. Preparation of Patterned and Multilayer Thin Films for Organic Electronics via Oxygen-Tolerant SI-PET-RAFT. Angewandte Chemie (International Ed. in English). PMID 34337845 DOI: 10.1002/anie.202107830 |
0.318 |
|
| 2021 |
Paisley NR, Halldorson SV, Tran MV, Gupta RM, Kamal S, Algar WR, Hudson ZM. Near-Infrared Emitting Boron Difluoride Curcuminoid-Based Polymers Exhibiting Thermally Activated Delayed Fluorescence as Biological Imaging Probes. Angewandte Chemie (International Ed. in English). PMID 34133838 DOI: 10.1002/anie.202103965 |
0.789 |
|
| 2020 |
Polgar AM, Tonge CM, Christopherson CJ, Paisley NR, Reyes AC, Hudson ZM. Thermally Assisted Fluorescent Polymers: Polycyclic Aromatic Materials for High Color Purity and White-Light Emission. Acs Applied Materials & Interfaces. 12: 38602-38613. PMID 32846499 DOI: 10.1021/Acsami.0C07892 |
0.795 |
|
| 2020 |
Mayder DM, Tonge CM, Hudson ZM. Thermally Activated Delayed Fluorescence in 1,3,4-Oxadiazoles with π-Extended Donors. The Journal of Organic Chemistry. PMID 32813517 DOI: 10.1021/Acs.Joc.0C00908 |
0.454 |
|
| 2020 |
Paisley NR, Tonge CM, Hudson ZM. Stimuli-Responsive Thermally Activated Delayed Fluorescence in Polymer Nanoparticles and Thin Films: Applications in Chemical Sensing and Imaging. Frontiers in Chemistry. 8: 229. PMID 32328478 DOI: 10.3389/Fchem.2020.00229 |
0.786 |
|
| 2020 |
Christopherson CJ, Mayder DM, Poisson J, Paisley NR, Tonge CM, Hudson ZM. 1,8-Naphthalimide-Based Polymers Exhibiting Deep-Red Thermally Activated Delayed Fluorescence and Their Application in Ratiometric Temperature Sensing. Acs Applied Materials & Interfaces. 12: 20000-20011. PMID 32310640 DOI: 10.1021/Acsami.0C05257 |
0.797 |
|
| 2020 |
Tonge CM, Paisley NR, Polgar AM, Lix K, Algar WR, Hudson ZM. Color-Tunable Thermally Activated Delayed Fluorescence in Oxadiazole-Based Acrylic Copolymers: Photophysical Properties and Applications in Ratiometric Oxygen Sensing. Acs Applied Materials & Interfaces. 12: 6525-6535. PMID 31989816 DOI: 10.1021/Acsami.9B22464 |
0.8 |
|
| 2020 |
Tonge CM, Zeng J, Zhao Z, Tang BZ, Hudson ZM. Bis(hexamethylazatriangulene)sulfone: a high-stability deep blue-violet fluorophore with 100% quantum yield and CIEy < 0.07 Journal of Materials Chemistry C. 8: 5150-5155. DOI: 10.1039/C9Tc05938E |
0.407 |
|
| 2020 |
Wright T, Petel Y, Zellman CO, Sauvé ER, Hudson ZM, Michal CA, Wolf MO. Room temperature crystallization of amorphous polysiloxane using photodimerization Chemical Science. 11: 3081-3088. DOI: 10.1039/C9Sc06235A |
0.363 |
|
| 2020 |
Paisley NR, Tonge CM, Mayder DM, Thompson KA, Hudson ZM. Tunable benzothiadiazole-based donor–acceptor materials for two-photon excited fluorescence Materials Chemistry Frontiers. 4: 555-566. DOI: 10.1039/C9Qm00627C |
0.779 |
|
| 2020 |
Shao F, Wang Y, Tonge CM, Sauvé ER, Hudson ZM. Self-assembly of luminescent triblock bottlebrush copolymers in solution Polymer Chemistry. 11: 1062-1071. DOI: 10.1039/C9Py01695C |
0.483 |
|
| 2020 |
Polgar AM, Poisson J, Paisley NR, Christopherson CJ, Reyes AC, Hudson ZM. Blue to Yellow Thermally Activated Delayed Fluorescence with Quantum Yields near Unity in Acrylic Polymers Based on D−π–A Pyrimidines Macromolecules. 53: 2039-2050. DOI: 10.1021/Acs.Macromol.0C00287 |
0.783 |
|
| 2020 |
Sauvé ER, Tonge CM, Hudson ZM. Organization of Chromophores into Multiblock Bottlebrush Nanofibers Allows for Regulation of Energy Transfer Processes Chemistry of Materials. 32: 2208-2219. DOI: 10.1021/Acs.Chemmater.0C00224 |
0.37 |
|
| 2019 |
Sauvé ER, Paeng J, Yamaguchi S, Hudson ZM. Donor-Acceptor Materials Exhibiting Thermally Activated Delayed Fluorescence Using a Planarized -Phenylbenzimidazole Acceptor. The Journal of Organic Chemistry. PMID 31738060 DOI: 10.1021/Acs.Joc.9B02283 |
0.432 |
|
| 2019 |
Sauvé ER, Tonge CM, Hudson ZM. Aggregation-Induced Energy Transfer in Color-Tunable Multiblock Bottlebrush Nanofibers. Journal of the American Chemical Society. 141: 16422-16431. PMID 31580661 DOI: 10.1021/Jacs.9B08133 |
0.436 |
|
| 2019 |
Tonge CM, Hudson ZM. Interface-Dependent Aggregation-Induced Delayed Fluorescence in Bottlebrush Polymer Nanofibers. Journal of the American Chemical Society. PMID 31441647 DOI: 10.1021/Jacs.9B07156 |
0.474 |
|
| 2019 |
Wang Y, Shao F, Sauvé ER, Tonge CM, Hudson ZM. Self-assembly of giant bottlebrush block copolymer surfactants from luminescent organic electronic materials. Soft Matter. PMID 31243420 DOI: 10.1039/C9Sm00931K |
0.586 |
|
| 2019 |
Tonge CM, Yuan F, Lu Z, Hudson ZM. Cu(0)-RDRP as an efficient and low-cost synthetic route to blue-emissive polymers for OLEDs Polymer Chemistry. 10: 3288-3297. DOI: 10.1039/C9Py00294D |
0.416 |
|
| 2019 |
Bajj DNF, Tran MV, Tsai H, Kim H, Paisley NR, Algar WR, Hudson ZM. Fluorescent Heterotelechelic Single-Chain Polymer Nanoparticles: Synthesis, Spectroscopy, and Cellular Imaging Acs Applied Nano Materials. 2: 898-909. DOI: 10.1021/ACSANM.8B02149 |
0.755 |
|
| 2018 |
Tonge CM, Sauve ER, Cheng S, Howard TA, Hudson ZM. Multiblock Bottlebrush Nanofibers from Organic Electronic Materials. Journal of the American Chemical Society. PMID 30180557 DOI: 10.1021/Jacs.8B07915 |
0.407 |
|
| 2018 |
Mayder DM, Thompson KA, Christopherson CJ, Paisley NR, Hudson ZM. An efficient room-temperature synthesis of highly phosphorescent styrenic Pt(ii) complexes and their polymerization by ATRP Polymer Chemistry. 9: 5418-5425. DOI: 10.1039/C8Py01337C |
0.764 |
|
| 2018 |
Tonge CM, Sauvé ER, Paisley NR, Heyes JE, Hudson ZM. Polymerization of acrylates based on n-type organic semiconductors using Cu(0)-RDRP Polymer Chemistry. 9: 3359-3367. DOI: 10.1039/C8Py00670A |
0.771 |
|
| 2018 |
Sauvé ER, Tonge CM, Paisley NR, Cheng S, Hudson ZM. Cu(0)-RDRP of acrylates based on p-type organic semiconductors Polymer Chemistry. 9: 1397-1403. DOI: 10.1039/C8Py00295A |
0.772 |
|
| 2018 |
Christopherson CJ, Hackett ZS, Sauvé ER, Paisley NR, Tonge CM, Mayder DM, Hudson ZM. Synthesis of phosphorescent iridium-containing acrylic monomers and their room-temperature polymerization by Cu(0)-RDRP Journal of Polymer Science Part a: Polymer Chemistry. 56: 2539-2546. DOI: 10.1002/Pola.29233 |
0.739 |
|
| 2018 |
Paisley NR, Tonge CM, Sauvé ER, Halldorson SV, Hudson ZM. Synthesis of polymeric organic semiconductors using semifluorinated polymer precursors Journal of Polymer Science Part A. 56: 2183-2191. DOI: 10.1002/Pola.29183 |
0.766 |
|
| 2017 |
Hao H, Thompson KA, Hudson ZM, Schafer L. Ti-Catalyzed Hydroamination for the Synthesis of Amine-Containing π-Conjugated Materials. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29282775 DOI: 10.1002/Chem.201704500 |
0.395 |
|
| 2017 |
Page ZA, Chiu C, Narupai B, Laitar DS, Mukhopadhyay S, Sokolov A, Hudson ZM, Bou Zerdan R, McGrath AJ, Kramer JW, Barton BE, Hawker CJ. Highly Photoluminescent Nonconjugated Polymers for Single-Layer Light Emitting Diodes Acs Photonics. 4: 631-641. DOI: 10.1021/Acsphotonics.6B00994 |
0.453 |
|
| 2015 |
Hudson ZM, Qian J, Boott CE, Winnik MA, Manners I. Fluorous Cylindrical Micelles of Controlled Length by Crystallization-Driven Self-Assembly of Block Copolymers in Fluorinated Media. Acs Macro Letters. 4: 187-191. PMID 35596429 DOI: 10.1021/mz500764n |
0.395 |
|
| 2015 |
Gould OE, Qiu H, Lunn DJ, Rowden J, Harniman RL, Hudson ZM, Winnik MA, Miles MJ, Manners I. Transformation and patterning of supermicelles using dynamic holographic assembly. Nature Communications. 6: 10009. PMID 26627644 DOI: 10.1038/Ncomms10009 |
0.45 |
|
| 2015 |
Qiu H, Hudson ZM, Winnik MA, Manners I. Micelle assembly. Multidimensional hierarchical self-assembly of amphiphilic cylindrical block comicelles. Science (New York, N.Y.). 347: 1329-32. PMID 25792323 DOI: 10.1126/Science.1261816 |
0.439 |
|
| 2015 |
Hudson ZM, Qian J, Boott CE, Winnik MA, Manners I. Fluorous cylindrical micelles of controlled length by crystallization-driven self-assembly of block copolymers in fluorinated media Acs Macro Letters. 4: 187-191. DOI: 10.1021/Mz500764N |
0.469 |
|
| 2015 |
Mattson KM, Latimer AA, McGrath AJ, Lynd NA, Lundberg P, Hudson ZM, Hawker CJ. A facile synthesis of catechol-functionalized poly(ethylene oxide) block and random copolymers Journal of Polymer Science, Part a: Polymer Chemistry. 53: 2685-2692. DOI: 10.1002/Pola.27749 |
0.408 |
|
| 2014 |
Finnegan JR, Lunn DJ, Gould OE, Hudson ZM, Whittell GR, Winnik MA, Manners I. Gradient crystallization-driven self-assembly: cylindrical micelles with "patchy" segmented coronas via the coassembly of linear and brush block copolymers. Journal of the American Chemical Society. 136: 13835-44. PMID 25243847 DOI: 10.1021/Ja507121H |
0.491 |
|
| 2014 |
Hudson ZM, Boott CE, Robinson ME, Rupar PA, Winnik MA, Manners I. Tailored hierarchical micelle architectures using living crystallization-driven self-assembly in two dimensions. Nature Chemistry. 6: 893-8. PMID 25242484 DOI: 10.1038/Nchem.2038 |
0.457 |
|
| 2014 |
Belzile MN, Wang X, Hudson ZM, Wang S. Impact of constitutional isomerism on phosphorescence and anion-sensing properties of donor-acceptor organoboron Pt(II) complexes. Dalton Transactions (Cambridge, England : 2003). 43: 13696-703. PMID 25100509 DOI: 10.1039/C4Dt01949K |
0.535 |
|
| 2014 |
Hudson ZM, Manners I. Chemistry. Assembly and disassembly of ferrocene-based nanotubes. Science (New York, N.Y.). 344: 482-3. PMID 24786069 DOI: 10.1126/Science.1254140 |
0.491 |
|
| 2014 |
Hudson ZM, Lunn DJ, Winnik MA, Manners I. Colour-tunable fluorescent multiblock micelles. Nature Communications. 5: 3372. PMID 24594554 DOI: 10.1038/Ncomms4372 |
0.538 |
|
| 2014 |
Qian J, Li X, Lunn DJ, Gwyther J, Hudson ZM, Kynaston E, Rupar PA, Winnik MA, Manners I. Uniform, high aspect ratio fiber-like micelles and block co-micelles with a crystalline π-conjugated polythiophene core by self-seeding. Journal of the American Chemical Society. 136: 4121-4. PMID 24564504 DOI: 10.1021/Ja500661K |
0.456 |
|
| 2012 |
Hudson ZM, Ko SB, Yamaguchi S, Wang S. Modulating the photoisomerization of N,C-chelate organoboranes with triplet acceptors. Organic Letters. 14: 5610-3. PMID 23092118 DOI: 10.1021/Ol302742G |
0.51 |
|
| 2012 |
Hudson ZM, Sun C, Helander MG, Chang YL, Lu ZH, Wang S. Highly efficient blue phosphorescence from triarylboron-functionalized platinum(II) complexes of N-heterocyclic carbenes. Journal of the American Chemical Society. 134: 13930-3. PMID 22891995 DOI: 10.1021/Ja3048656 |
0.548 |
|
| 2012 |
Hudson ZM, Wang Z, Helander MG, Lu ZH, Wang S. N-heterocyclic carbazole-based hosts for simplified single-layer phosphorescent OLEDs with high efficiencies. Advanced Materials (Deerfield Beach, Fla.). 24: 2922-8. PMID 22553162 DOI: 10.1002/Adma.201200927 |
0.521 |
|
| 2012 |
Sun C, Hudson ZM, Chen LD, Wang S. Double cyclization/aryl migration across an alkyne bond enabled by organoboryl and diarylplatinum groups. Angewandte Chemie (International Ed. in English). 51: 5671-4. PMID 22539452 DOI: 10.1002/Anie.201201781 |
0.452 |
|
| 2012 |
Hudson ZM, Blight BA, Wang S. Efficient and high yield one-pot synthesis of cyclometalated platinum(II) β-diketonates at ambient temperature. Organic Letters. 14: 1700-3. PMID 22414237 DOI: 10.1021/Ol300242F |
0.536 |
|
| 2011 |
Hudson ZM, Wang S. Metal-containing triarylboron compounds for optoelectronic applications. Dalton Transactions (Cambridge, England : 2003). 40: 7805-16. PMID 21603687 DOI: 10.1039/C1Dt10292C |
0.576 |
|
| 2011 |
Hudson ZM, Sun C, Harris KJ, Lucier BE, Schurko RW, Wang S. Probing the structural origins of vapochromism of a triarylboron-functionalized platinum(II) acetylide by optical and multinuclear solid-state NMR spectroscopy. Inorganic Chemistry. 50: 3447-57. PMID 21425806 DOI: 10.1021/Ic102349H |
0.527 |
|
| 2011 |
Sun Y, Hudson ZM, Rao Y, Wang S. Tuning and switching MLCT phosphorescence of [Ru(bpy)3]2+ complexes with triarylboranes and anions. Inorganic Chemistry. 50: 3373-8. PMID 21413739 DOI: 10.1021/Ic1021966 |
0.521 |
|
| 2011 |
Zlojutro V, Sun Y, Hudson ZM, Wang S. Triarylboron-functionalized 8-hydroxyquinolines and their aluminium(III) complexes. Chemical Communications (Cambridge, England). 47: 3837-9. PMID 21321693 DOI: 10.1039/C0Cc04573J |
0.525 |
|
| 2011 |
Hudson ZM, Liu XY, Wang S. Switchable three-state fluorescence of a nonconjugated donor-acceptor triarylborane. Organic Letters. 13: 300-3. PMID 21142199 DOI: 10.1021/Ol102749Y |
0.561 |
|
| 2011 |
Hudson ZM, Helander MG, Lu ZH, Wang S. Highly efficient orange electrophosphorescence from a trifunctional organoboron-Pt(II) complex. Chemical Communications (Cambridge, England). 47: 755-7. PMID 21069240 DOI: 10.1039/C0Cc04014B |
0.514 |
|
| 2011 |
Wang ZB, Helander MG, Hudson ZM, Qiu J, Wang S, Lu ZH. Pt(II) complex based phosphorescent organic light emitting diodes with external quantum efficiencies above 20% Applied Physics Letters. 98: 213301. DOI: 10.1063/1.3593495 |
0.555 |
|
| 2011 |
Wang ZB, Helander MG, Qiu J, Puzzo DP, Greiner MT, Hudson ZM, Wang S, Liu ZW, Lu ZH. Unlocking the full potential of organic light-emitting diodes on flexible plastic Nature Photonics. 5: 753-757. DOI: 10.1038/Nphoton.2011.259 |
0.532 |
|
| 2011 |
Sun C, Hudson ZM, Helander MG, Lu Z, Wang S. A Polyboryl-Functionalized Triazine as an Electron Transport Material for OLEDs Organometallics. 30: 5552-5555. DOI: 10.1021/Om2007979 |
0.524 |
|
| 2011 |
Hudson ZM, Wang S. Nonconjugated Dimesitylboryl-Functionalized Phenylpyridines and Their Cyclometalated Platinum(II) Complexes Organometallics. 30: 4695-4701. DOI: 10.1021/Om200539R |
0.529 |
|
| 2010 |
White W, Hudson ZM, Feng X, Han S, Lu ZH, Wang S. Linear and star-shaped benzimidazolyl derivatives: syntheses, photophysical properties and use as highly efficient electron transport materials in OLEDs. Dalton Transactions (Cambridge, England : 2003). 39: 892-9. PMID 20066234 DOI: 10.1039/B918203A |
0.594 |
|
| 2010 |
Wang N, Hudson ZM, Wang S. Reactivity of Aryldimesitylboranes under Suzuki−Miyaura Coupling Conditions Organometallics. 29: 4007-4011. DOI: 10.1021/Om1006903 |
0.489 |
|
| 2010 |
Hudson ZM, Sun C, Helander MG, Amarne H, Lu Z, Wang S. Enhancing Phosphorescence and Electrophosphorescence Efficiency of Cyclometalated Pt(II) Compounds with Triarylboron Advanced Functional Materials. 20: 3426-3439. DOI: 10.1002/Adfm.201000904 |
0.56 |
|
| 2009 |
Baik C, Hudson ZM, Amarne H, Wang S. Enhancing the photochemical stability of N,C-chelate boryl compounds: C-C bond formation versus C=C bond cis,trans-isomerization. Journal of the American Chemical Society. 131: 14549-59. PMID 19769363 DOI: 10.1021/Ja906430S |
0.498 |
|
| 2009 |
Hudson ZM, Sun Y, Ross B, Wang RY, Wang S. The anionic coordination polymer {K2[Pt(II)2Ag(I)8(2,2'-bipyridine)2(O2CCF3)14]}n. Acta Crystallographica. Section C, Crystal Structure Communications. 65: m328-30. PMID 19652314 DOI: 10.1107/S010827010902839X |
0.526 |
|
| 2009 |
Hudson ZM, Wang S. Impact of donor-acceptor geometry and metal chelation on photophysical properties and applications of triarylboranes. Accounts of Chemical Research. 42: 1584-96. PMID 19558183 DOI: 10.1021/Ar900072U |
0.567 |
|
| 2009 |
Hudson ZM, Zhao SB, Wang RY, Wang S. Switchable ambient-temperature singlet-triplet dual emission in nonconjugated donor-acceptor triarylboron-Pt(II) complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 6131-7. PMID 19472234 DOI: 10.1002/Chem.200900641 |
0.547 |
|
| 2009 |
Hudson Z, Zhao S, Wang R, Wang S. Cover Picture: Switchable Ambient-Temperature Singlet-Triplet Dual Emission in Nonconjugated Donor-Acceptor Triarylboron-PtIIComplexes (Chem. Eur. J. 25/2009) Chemistry - a European Journal. 15: 6083-6083. DOI: 10.1002/Chem.200990091 |
0.557 |
|
| 2008 |
Zhao SB, Wucher P, Hudson ZM, McCormick TM, Liu XY, Suning W, Feng XD, Lu ZH. Impact of the linker on the electronic and luminescent properties of diboryl compounds: Molecules with two BMes2 Groups and the peculiar behavior of l,6-(BMes2)2pyrene Organometallics. 27: 6446-6456. DOI: 10.1021/Om800856G |
0.313 |
|
| Show low-probability matches. |