Year |
Citation |
Score |
2016 |
Kanimozhi C, Kim M, Larson SR, Choi JW, Choo Y, Sweat DP, Osuji CO, Gopalan P. Isomeric Effect Enabled Thermally Driven Self-Assembly of Hydroxystyrene-Based Block Copolymers. Acs Macro Letters. 5: 833-838. PMID 35614756 DOI: 10.1021/acsmacrolett.6b00376 |
0.591 |
|
2016 |
Choi JW, Li Z, Black CT, Sweat DP, Wang X, Gopalan P. Patterning at the 10 nanometer length scale using a strongly segregating block copolymer thin film and vapor phase infiltration of inorganic precursors. Nanoscale. PMID 27216015 DOI: 10.1039/C6Nr01409G |
0.586 |
|
2016 |
Kanimozhi C, Kim M, Larson SR, Choi JW, Choo Y, Sweat DP, Osuji CO, Gopalan P. Isomeric Effect Enabled Thermally Driven Self-Assembly of Hydroxystyrene-Based Block Copolymers Acs Macro Letters. 5: 833-838. DOI: 10.1021/Acsmacrolett.6B00376 |
0.613 |
|
2014 |
Sweat DP, Kim M, Larson SR, Choi JW, Choo Y, Osuji CO, Gopalan P. Rational design of a block copolymer with a high interaction parameter Macromolecules. 47: 6687-6696. DOI: 10.1021/Ma501597G |
0.632 |
|
2014 |
Sweat DP, Kim M, Schmitt AK, Perroni DV, Fry CG, Mahanthappa MK, Gopalan P. Phase behavior of poly(4-hydroxystyrene-block-styrene) synthesized by living anionic polymerization of an acetal protected monomer Macromolecules. 47: 6302-6310. DOI: 10.1021/Ma501126T |
0.637 |
|
2014 |
Sweat DP, Yu X, Kim M, Gopalan P. Synthesis of poly(4-hydroxystyrene)-based block copolymers containing acid-sensitive blocks by living anionic polymerization Journal of Polymer Science, Part a: Polymer Chemistry. 52: 1458-1468. DOI: 10.1002/Pola.27138 |
0.64 |
|
2013 |
Sweat DP, Kim M, Yu X, Schmitt SK, Han E, Choi JW, Gopalan P. A dual functional layer for block copolymer self-assembly and the growth of nanopatterned polymer brushes. Langmuir : the Acs Journal of Surfaces and Colloids. 29: 12858-65. PMID 24053350 DOI: 10.1021/La403474K |
0.693 |
|
2013 |
Sweat DP, Kim M, Yu X, Gopalan P. A single-component inimer containing cross-linkable ultrathin polymer coating for dense polymer brush growth. Langmuir : the Acs Journal of Surfaces and Colloids. 29: 3805-12. PMID 23425347 DOI: 10.1021/La305060Z |
0.632 |
|
2013 |
Kim M, Han E, Sweat DP, Gopalan P. Interplay of surface chemical composition and film thickness on graphoepitaxial assembly of asymmetric block copolymers Soft Matter. 9: 6135-6141. DOI: 10.1039/C3Sm50307K |
0.647 |
|
2012 |
Paoprasert P, Kandala S, Sweat DP, Ruther R, Gopalan P. Versatile grafting chemistry for creation of stable molecular layers on oxides Journal of Materials Chemistry. 22: 1046-1053. DOI: 10.1039/C1Jm13293H |
0.625 |
|
2009 |
Steckler TT, Zhang X, Hwang J, Honeyager R, Ohira S, Zhang XH, Grant A, Ellinger S, Odom SA, Sweat D, Tanner DB, Rinzler AG, Barlow S, Brédas JL, Kippelen B, et al. A spray-processable, low bandgap, and ambipolar donor-acceptor conjugated polymer. Journal of the American Chemical Society. 131: 2824-6. PMID 19199436 DOI: 10.1021/Ja809372U |
0.319 |
|
Low-probability matches (unlikely to be authored by this person) |
2011 |
Suthiwangcharoen N, Pochini SM, Sweat DP, Stephens CE. An intramolecular N-arylation approach to 3-functionalized 4,9-dihydropyrrolo[2,1-b]quinazolines Journal of Heterocyclic Chemistry. 48: 706-709. DOI: 10.1002/jhet.534 |
0.109 |
|
2008 |
Sweat DP, Stephens CE. A modified synthesis of tellurophene using NaBH4 to generate sodium telluride Journal of Organometallic Chemistry. 693: 2463-2464. DOI: 10.1016/j.jorganchem.2008.04.022 |
0.102 |
|
2009 |
Sweat DP, Stephens CE. Synthesis and stille cross-coupling reactions of 2-(tributylstannyl)-and 2,5-bis(trimethylstannyl)tellurophene Synthesis. 3214-3218. DOI: 10.1055/s-0029-1216958 |
0.078 |
|
2019 |
Depauw S, Lambert M, Jambon S, Paul A, Peixoto P, Nhili R, Marongiu L, Figeac M, Dassi C, Paul-Constant C, Billoré B, Kumar A, Farahat AA, Ismail MA, Mineva E, ... Sweat DP, et al. Heterocyclic Diamidine DNA ligands as HOXA9 Transcription Factor Inhibitors: Design, Molecular Evaluation and Cellular Consequences in HOXA9-Dependant Leukemia Cell Model. Journal of Medicinal Chemistry. PMID 30645099 DOI: 10.1021/Acs.Jmedchem.8B01448 |
0.047 |
|
Hide low-probability matches. |