Year |
Citation |
Score |
2020 |
Zhang G, Gautam P, Chan JMW. Symmetrical and unsymmetrical fluorine-rich ullazines via controlled cycloaromatizations Organic Chemistry Frontiers. 7: 787-795. DOI: 10.1039/D0Qo00033G |
0.323 |
|
2019 |
Niu X, Gautam P, Kuang Z, Yu CP, Guo Y, Song H, Guo Q, Chan JMW, Xia A. Intramolecular charge transfer and solvation dynamics of push-pull dyes with different π-conjugated linkers. Physical Chemistry Chemical Physics : Pccp. PMID 31353370 DOI: 10.1039/C9Cp02559F |
0.428 |
|
2018 |
Gautam P, Wang Y, Zhang G, Sun H, Chan JMW. Using the Negative Hyperconjugation Effect of Pentafluorosulfanyl Acceptors to Enhance Two-Photon Absorption in Push–Pull Chromophores Chemistry of Materials. 30: 7055-7066. DOI: 10.1021/Acs.Chemmater.8B02723 |
0.404 |
|
2017 |
Gautam P, Yu CP, Zhang G, Hillier VE, Chan JMW. Pulling with the Pentafluorosulfanyl (SF5) Acceptor in Push-Pull Dyes. The Journal of Organic Chemistry. PMID 28945090 DOI: 10.1021/Acs.Joc.7B01972 |
0.447 |
|
2017 |
Rout Y, Gautam P, Misra R. Unsymmetrical and symmetrical push-pull phenothiazines. The Journal of Organic Chemistry. PMID 28587457 DOI: 10.1021/Acs.Joc.7B00991 |
0.782 |
|
2017 |
D'Souza F, Gautam P, Misra R, Thomas M. Ultrafast charge separation in triphenylamine-BODIPY derived triads carrying centrally positioned, highly electron deficient, dicyanoquinodimethane or tetracyanobutadiene acceptors. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28486754 DOI: 10.1002/Chem.201701604 |
0.668 |
|
2017 |
Gautam P, Sharma R, Misra R, Keshtov ML, Kuklin SA, Sharma GD. Donor-acceptor-acceptor (D-A-A) type 1,8-naphthalimides as non-fullerene small molecule acceptors for bulk heterojunction solar cells. Chemical Science. 8: 2017-2024. PMID 28451319 DOI: 10.1039/C6Sc04461A |
0.624 |
|
2017 |
Poddar M, Gautam P, Rout Y, Misra R. Donor–acceptor phenothiazine functionalized BODIPYs Dyes and Pigments. 146: 368-373. DOI: 10.1016/J.Dyepig.2017.07.017 |
0.756 |
|
2016 |
Gautam P, Misra R, Biswas S, Sharma GD. A D-π-A1-π-A2 push-pull small molecule donor for solution processed bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics : Pccp. PMID 27149659 DOI: 10.1039/C6Cp01163B |
0.659 |
|
2016 |
Gautam P, Misra R, Sharma GD. Dicyanoquinodimethane-substituted benzothiadiazole for efficient small-molecule solar cells. Physical Chemistry Chemical Physics : Pccp. 18: 7235-41. PMID 26890875 DOI: 10.1039/C6Cp00243A |
0.594 |
|
2016 |
Maragani R, Gautam P, Mobin SM, Misra R. C2-Symmetric ferrocenyl bisthiazoles: synthesis, photophysical, electrochemical and DFT studies. Dalton Transactions (Cambridge, England : 2003). 45: 4802-9. PMID 26866584 DOI: 10.1039/C5Dt04988A |
0.695 |
|
2016 |
Gautam P, Misra R, Sharma GD. Dicyanoquinodimethane-substituted benzothiadiazole for efficient small-molecule solar cells Physical Chemistry Chemical Physics. 18: 7235-7241. DOI: 10.1039/c6cp00243a |
0.516 |
|
2015 |
Gautam P, Misra R, Siddiqui SA, Sharma GD. Unsymmetrical Donor-Acceptor-Acceptor-π-Donor Type Benzothiadiazole-Based Small Molecule for a Solution Processed Bulk Heterojunction Organic Solar Cell. Acs Applied Materials & Interfaces. 7: 10283-92. PMID 25946406 DOI: 10.1021/Acsami.5B02250 |
0.616 |
|
2015 |
Misra R, Maragani R, Pathak B, Gautam P, Mobin SM. Star shaped ferrocenyl substituted triphenylamines Rsc Advances. 5: 71046-71051. DOI: 10.1039/C5Ra13400E |
0.696 |
|
2015 |
Sharma R, Gautam P, Misra R, Shukla SK. β-Substituted triarylborane appended porphyrins: Photophysical properties and anion sensing Rsc Advances. 5: 27069-27074. DOI: 10.1039/C5Ra03931B |
0.722 |
|
2015 |
Gautam P, Maragani R, Misra R. Aryl-substituted symmetrical and unsymmetrical benzothiadiazoles Rsc Advances. 5: 18288-18294. DOI: 10.1039/C4Ra15424J |
0.679 |
|
2015 |
Misra R, Gautam P, Maragani R. Ferrocenyl thiazoles: Synthesis and properties Tetrahedron Letters. 56: 1664-1666. DOI: 10.1016/J.Tetlet.2015.02.031 |
0.694 |
|
2015 |
Gautam P, Misra R, Koukaras EN, Sharma A, Sharma GD. Donor-acceptor-acceptor-donor small molecules for solution processed bulk heterojunction solar cells Organic Electronics: Physics, Materials, Applications. 27: 72-83. DOI: 10.1016/J.Orgel.2015.09.006 |
0.376 |
|
2015 |
Gautam P, Misra R, Siddiqui SA, Sharma GD. Donor-acceptor-π-acceptor based charge transfer chromophore as electron donors for solution processed small molecule organic bulk heterojunction solar cells Organic Electronics: Physics, Materials, Applications. 19: 76-82. DOI: 10.1016/J.Orgel.2015.01.032 |
0.613 |
|
2015 |
Misra R, Gautam P. Meso-tetrakis(ferrocenylethynylphenyl) porphyrins: Synthesis and properties Journal of Organometallic Chemistry. 776: 83-88. DOI: 10.1016/J.Jorganchem.2014.11.006 |
0.599 |
|
2014 |
Misra R, Jadhav T, Dhokale B, Gautam P, Sharma R, Maragani R, Mobin SM. Carbazole-BODIPY conjugates: design, synthesis, structure and properties. Dalton Transactions (Cambridge, England : 2003). 43: 13076-86. PMID 25043199 DOI: 10.1039/C4Dt00983E |
0.771 |
|
2014 |
Misra R, Gautam P. Tuning of the HOMO-LUMO gap of donor-substituted symmetrical and unsymmetrical benzothiadiazoles. Organic & Biomolecular Chemistry. 12: 5448-57. PMID 24940822 DOI: 10.1039/C4Ob00629A |
0.677 |
|
2014 |
Gautam P, Maragani R, Mobin SM, Misra R. Reversible mechanochromism in dipyridylamine-substituted unsymmetrical benzothiadiazoles Rsc Advances. 4: 52526-52529. DOI: 10.1039/C4Ra09921D |
0.624 |
|
2014 |
Misra R, Maragani R, Gautam P, Mobin SM. Tetracyanoethylene substituted triphenylamine analogues Tetrahedron Letters. 55: 7102-7105. DOI: 10.1016/J.Tetlet.2014.10.148 |
0.657 |
|
2014 |
Gautam P, Maragani R, Misra R. Tuning the HOMO-LUMO gap of donor-substituted benzothiazoles Tetrahedron Letters. 55: 6827-6830. DOI: 10.1016/J.Tetlet.2014.10.094 |
0.702 |
|
2013 |
Misra R, Gautam P, Mobin SM. Aryl-substituted unsymmetrical benzothiadiazoles: synthesis, structure, and properties. The Journal of Organic Chemistry. 78: 12440-52. PMID 24274961 DOI: 10.1021/Jo402111Q |
0.686 |
|
2013 |
Misra R, Gautam P, Jadhav T, Mobin SM. Donor-acceptor ferrocenyl-substituted benzothiadiazoles: synthesis, structure, and properties. The Journal of Organic Chemistry. 78: 4940-8. PMID 23627745 DOI: 10.1021/Jo4005734 |
0.802 |
|
2013 |
Sharma R, Gautam P, Mobin SM, Misra R. β-Substituted ferrocenyl porphyrins: synthesis, structure, and properties. Dalton Transactions (Cambridge, England : 2003). 42: 5539-45. PMID 23440020 DOI: 10.1039/C3Dt00003F |
0.765 |
|
2013 |
Dhokale B, Gautam P, Mobin SM, Misra R. Donor-acceptor, ferrocenyl substituted BODIPYs with marvelous supramolecular interactions. Dalton Transactions (Cambridge, England : 2003). 42: 1512-8. PMID 23135611 DOI: 10.1039/C2Dt31632C |
0.786 |
|
2013 |
Misra R, Gautam P, Sharma R, Mobin SM. Donor–π–acceptor–π–donor ferrocenyl benzothiadiazoles: synthesis, structure, and properties Tetrahedron Letters. 54: 381-383. DOI: 10.1016/J.Tetlet.2012.11.016 |
0.747 |
|
2012 |
Gautam P, Dhokale B, Mobin SM, Misra R. Ferrocenyl BODIPYs: synthesis, structure and properties Rsc Advances. 2: 12105. DOI: 10.1039/C2Ra21964F |
0.791 |
|
2012 |
Dhokale B, Gautam P, Misra R. Donor–acceptor perylenediimide–ferrocene conjugates: synthesis, photophysical, and electrochemical properties Tetrahedron Letters. 53: 2352-2354. DOI: 10.1016/J.Tetlet.2012.02.107 |
0.781 |
|
2012 |
Gautam P, Dhokale B, Shukla V, Singh CP, Bindra KS, Misra R. Optical limiting performance of meso-tetraferrocenyl porphyrin and its metal derivatives Journal of Photochemistry and Photobiology a: Chemistry. 239: 24-27. DOI: 10.1016/J.Jphotochem.2012.04.020 |
0.744 |
|
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