Year |
Citation |
Score |
2023 |
De S, Asthana D, Thirmal C, Keshri SK, Ghosh RK, Hundal G, Kumar R, Singh S, Chatterjee R, Mukhopadhyay P. A folded π-system with supramolecularly oriented dipoles: single-component piezoelectric relaxor with NLO activity. Chemical Science. 14: 2547-2552. PMID 36908941 DOI: 10.1039/d2sc06141d |
0.742 |
|
2021 |
Mukhopadhyay P, Keshri SK, Mandal K, Kumar Y, Yadav D. Naphthalenediimides with High Fluorescence Quantum Yield: Bright-Red, Stable and Responsive Fluorescent Dyes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33539577 DOI: 10.1002/chem.202100020 |
0.742 |
|
2020 |
Mukhopadhyay P, Mandal K, Bansal D, Kumar Y, Shukla J, Niazi R. Halogen Bonded Assemblies of Arylene-imides and -diimides: Insight from Electronic, Structural and Computational studies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32428280 DOI: 10.1002/Chem.202001706 |
0.345 |
|
2020 |
Shukla J, Kumar S, Rustam, Mukhopadhyay P. Synthesis of Stable, High-SOMO Zwitterionic Radicals: Enabling Intermolecular Electron Transfer between Naphthalenediimides. Organic Letters. PMID 32356990 DOI: 10.1021/Acs.Orglett.0C01263 |
0.348 |
|
2020 |
Shukla J, Singh VP, Mukhopadhyay P. Molecular and Supramolecular Multiredox Systems. Chemistryopen. 9: 304-324. PMID 32154051 DOI: 10.1002/Open.201900339 |
0.314 |
|
2019 |
Kumar S, Shukla J, Mandal K, Kumar Y, Prakash R, Ram P, Mukhopadhyay P. Doubly zwitterionic, di-reduced, highly electron-rich, air-stable naphthalenediimides: redox-switchable islands of aromatic-antiaromatic states. Chemical Science. 10: 6482-6493. PMID 31341600 DOI: 10.1039/C9Sc00962K |
0.355 |
|
2019 |
Kumar Y, Kumar S, Bansal D, Mukhopadhyay P. Synthesis and Isolation of a Stable Perylenediimide Radical Anion and Its Exceptionally Electron-Deficient Precursor. Organic Letters. PMID 30869910 DOI: 10.1021/Acs.Orglett.9B00490 |
0.359 |
|
2019 |
Mukhopadhyay P, Kumar S, Malik V, Shukla J, Kumar Y, Bansal D, Chatterjee R. Ionic Assembly, Anion-π, Magnetic and Electronic Attributes of Ambient Stable Naphthalenediimide Radical Ions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30702792 DOI: 10.1002/Chem.201805978 |
0.328 |
|
2019 |
Bansal D, Kumar Y, Rustam, Kumar S, Mandal K, Hundal G, Mukhopadhyay P. Core-insertion of palladium in naphthalenediimides: Opto-electronic properties, structural insights and coupling studies Inorganica Chimica Acta. 486: 185-192. DOI: 10.1016/J.Ica.2018.09.077 |
0.312 |
|
2018 |
Mukhopadhyay P, Kumar Y, Kumar S, Mandal K. Isolation of Tetracyano-Naphthalenediimide and its Ambient Stable Planar Radical Anion. Angewandte Chemie (International Ed. in English). PMID 30260056 DOI: 10.1002/Anie.201807836 |
0.332 |
|
2018 |
Shukla J, Ajayakumar MR, Kumar Y, Mukhopadhyay P. Electron sponge from naphthalenediimide-viologen conjugates: water-stable, highly electron-deficient polyions with 1 V potential window. Chemical Communications (Cambridge, England). PMID 29303183 DOI: 10.1039/C7Cc09372A |
0.353 |
|
2018 |
Kumar S, Shukla J, Kumar Y, Mukhopadhyay P. Electron-poor arylenediimides Organic Chemistry Frontiers. 5: 2254-2276. DOI: 10.1039/C8Qo00256H |
0.319 |
|
2018 |
Jassal AK, Sran BS, Mandal K, Mukhopadhyay P, Hundal G. Role Reversal of the Carboxylate Group from Coordination to Hydrogen Bonding Only, in Structurally Diverse Metal-2-amino,5-Nitro-benzoates: A First Report Crystal Growth & Design. 18: 4737-4748. DOI: 10.1021/Acs.Cgd.8B00771 |
0.326 |
|
2017 |
Mukhopadhyay P, Keshri SK, Asthana D, Chorol S, Kumar Y. Appending Diverse -Extended Acceptors with TTF Donors: Multistate Redox, Radical Ion Generation and Mid-IR Absorbing Mixed-Valence States. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29077995 DOI: 10.1002/Chem.201704604 |
0.755 |
|
2017 |
Mukhopadhyay P, Keshri SK, Kumar S, Mandal K. Ambient Water Stable Dianionic Electron Donors: Intramolecular Noncovalent Conduits Assist Charge Delocalization. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28609606 DOI: 10.1002/Chem.201701868 |
0.74 |
|
2017 |
Keshri SK, Kumar S, Mandal K, Mukhopadhyay P. Frontispiece: Ambient Water-Stable Dianionic Electron Donors: Intramolecular Noncovalent Conduits Assist Charge Delocalization Chemistry - a European Journal. 23. DOI: 10.1002/Chem.201784964 |
0.308 |
|
2016 |
Dana S, Keshri SK, Shukla J, Vikramdeo KS, Mondal N, Mukhopadhyay P, Dhar SK. Design, Synthesis and Evaluation of Bifunctional Acridinine-Naphthalenediimide Redox-Active Conjugates as Antimalarials. Acs Omega. 1: 318-333. PMID 30023479 DOI: 10.1021/acsomega.6b00060 |
0.738 |
|
2016 |
Kumar Y, Kumar S, Kumar Keshri S, Shukla J, Singh SS, Thakur TS, Denti M, Facchetti A, Mukhopadhyay P. Synthesis of Octabromoperylene Dianhydride and Diimides: Evidence of Halogen Bonding and Semiconducting Properties. Organic Letters. PMID 26771262 DOI: 10.1021/Acs.Orglett.5B03513 |
0.352 |
|
2015 |
Asthana D, Shukla J, Dana S, Rani V, Ajayakumar MR, Rawat K, Mandal K, Yadav P, Ghosh S, Mukhopadhyay P. Assorted morphosynthesis: access to multi-faceted nano-architectures from a super-responsive dual π-functional amphiphilic construct. Chemical Communications (Cambridge, England). PMID 26194349 DOI: 10.1039/C5Cc05198C |
0.353 |
|
2014 |
Kumar S, Ajayakumar MR, Hundal G, Mukhopadhyay P. Extraordinary stability of naphthalenediimide radical ion and its ultra-electron-deficient precursor: strategic role of the phosphonium group. Journal of the American Chemical Society. 136: 12004-10. PMID 25093533 DOI: 10.1021/Ja504903J |
0.353 |
|
2014 |
Asthana D, Keshri SK, Hundal G, Sharma G, Mukhopadhyay P. Self-assembly patterns of steroid-based all-organic ferroelectrics: Valuable insights from the single-crystals derived from an organogel and solution Crystengcomm. 16: 4861-4866. DOI: 10.1039/C4Ce00013G |
0.326 |
|
2014 |
Asthana D, Hundal G, Mukhopadhyay P. Self-assembly characteristics of a multipolar donor-acceptor-based bis-pyrene integrated molecular tweezer Journal of Chemical Sciences. 126: 1331-1336. DOI: 10.1007/S12039-014-0687-8 |
0.402 |
|
2013 |
Ajayakumar MR, Mandal K, Rawat K, Asthana D, Pandey R, Sharma A, Yadav S, Ghosh S, Mukhopadhyay P. Single electron transfer-driven multi-dimensional signal read-out function of TCNQ as an "off-the-shelf" detector for cyanide. Acs Applied Materials & Interfaces. 5: 6996-7000. PMID 23721131 DOI: 10.1021/Am4011176 |
0.305 |
|
2013 |
Asthana D, Pandey R, Mukhopadhyay P. Urea-based constructs readily amplify and attenuate nonlinear optical activity in response to H-bonding and anion recognition. Chemical Communications (Cambridge, England). 49: 451-3. PMID 23108038 DOI: 10.1039/C2Cc36631B |
0.335 |
|
2013 |
Ghosh S, Mukhopadhyay P, Isaacs L. Deconvolution of a multi-component interaction network using systems chemistry Journal of Systems Chemistry. 1. DOI: 10.1186/1759-2208-1-6 |
0.626 |
|
2012 |
Ajayakumar MR, Asthana D, Mukhopadhyay P. Core-modified naphthalenediimides generate persistent radical anion and cation: new panchromatic NIR probes. Organic Letters. 14: 4822-5. PMID 22954312 DOI: 10.1021/Ol302140X |
0.305 |
|
2012 |
Asthana D, Ajayakumar MR, Pant RP, Mukhopadhyay P. NTCDA-TTF first axial fusion: emergent panchromatic, NIR optical, multi-state redox and high optical contrast photooxidation. Chemical Communications (Cambridge, England). 48: 6475-7. PMID 22540127 DOI: 10.1039/C2Cc31274C |
0.306 |
|
2011 |
Sukul PK, Asthana D, Mukhopadhyay P, Summa D, Muccioli L, Zannoni C, Beljonne D, Rowan AE, Malik S. Assemblies of perylene diimide derivatives with melamine into luminescent hydrogels. Chemical Communications (Cambridge, England). 47: 11858-60. PMID 21971484 DOI: 10.1039/C1Cc14189A |
0.622 |
|
2011 |
Asthana D, Kumar A, Pathak A, Sukul PK, Malik S, Chatterjee R, Patnaik S, Rissanen K, Mukhopadhyay P. An all-organic steroid-D-Ï€-A modular design drives ferroelectricity in supramolecular solids and nano-architectures at RT. Chemical Communications (Cambridge, England). 47: 8928-30. PMID 21709861 DOI: 10.1039/C1Cc12398J |
0.604 |
|
2011 |
Sukul PK, Asthana D, Mukhopadhyay P, Summa D, Muccioli L, Zannoni C, Beljonne D, Rowan AE, Malik S. Assemblies of perylene diimide derivatives with melamine into luminescent hydrogels Chemical Communications. 47: 11858-11860. DOI: 10.1039/c1cc14189a |
0.583 |
|
2010 |
Mukhopadhyay P, Fujita N, Takada A, Kishida T, Shirakawa M, Shinkai S. Regulation of a real-time self-healing process in organogel tissues by molecular adhesives. Angewandte Chemie (International Ed. in English). 49: 6338-42. PMID 20661973 DOI: 10.1002/Anie.201001382 |
0.394 |
|
2010 |
Ajayakumar MR, Mukhopadhyay P, Yadav S, Ghosh S. Single-electron transfer driven cyanide sensing: a new multimodal approach. Organic Letters. 12: 2646-9. PMID 20455554 DOI: 10.1021/Ol1008558 |
0.326 |
|
2007 |
Chakrabarti S, Mukhopadhyay P, Lin S, Isaacs L. Reconfigurable four-component molecular switch based on pH-controlled guest swapping. Organic Letters. 9: 2349-52. PMID 17500562 DOI: 10.1021/Ol070730C |
0.514 |
|
2007 |
Malik S, Fujita N, Mukhopadhyay P, Goto Y, Kaneko K, Ikeda T, Shinkai S. Creation of 1D [60]fullerene superstructures and its polymerization by γ-ray irradiation J. Mater. Chem.. 17: 2454-2458. DOI: 10.1039/B701583F |
0.64 |
|
2006 |
Mukhopadhyay P, Zavalij PY, Isaacs L. High fidelity kinetic self-sorting in multi-component systems based on guests with multiple binding epitopes. Journal of the American Chemical Society. 128: 14093-102. PMID 17061892 DOI: 10.1021/Ja063390J |
0.539 |
|
2006 |
Mukhopadhyay P, Iwashita Y, Shirakawa M, Kawano S, Fujita N, Shinkai S. Spontaneous colorimetric sensing of the positional isomers of dihydroxynaphthalene in a 1D organogel matrix. Angewandte Chemie (International Ed. in English). 45: 1592-5. PMID 16470894 DOI: 10.1002/Anie.200503158 |
0.372 |
|
2006 |
Bag B, Mukhopadhyay P, Bharadwaj PK. Fluorescence signaling systems with a cryptand receptor incorporating electron-withdrawing groups: Metal ion specificity and solvent dependence Journal of Photochemistry and Photobiology a: Chemistry. 181: 215-225. DOI: 10.1016/J.Jphotochem.2005.12.001 |
0.551 |
|
2005 |
Liu S, Ruspic C, Mukhopadhyay P, Chakrabarti S, Zavalij PY, Isaacs L. The cucurbit[n]uril family: prime components for self-sorting systems. Journal of the American Chemical Society. 127: 15959-67. PMID 16277540 DOI: 10.1021/Ja055013X |
0.559 |
|
2005 |
Lagona J, Mukhopadhyay P, Chakrabarti S, Isaacs L. The cucurbit[n]uril family. Angewandte Chemie (International Ed. in English). 44: 4844-70. PMID 16052668 DOI: 10.1002/Anie.200460675 |
0.733 |
|
2005 |
Lagona J, Mukhopadhyay P, Chakrabarti S, Isaacs L. Die Cucurbit[n]uril‐Familie Angewandte Chemie. 117: 4922-4949. DOI: 10.1002/Ange.200460675 |
0.711 |
|
2004 |
Mukhopadhyay P, Wu A, Isaacs L. Social self-sorting in aqueous solution. The Journal of Organic Chemistry. 69: 6157-64. PMID 15357573 DOI: 10.1021/Jo049976A |
0.556 |
|
2004 |
Wu A, Mukhopadhyay P, Chakraborty A, Fettinger JC, Isaacs L. Molecular clips form isostructural dimeric aggregates from benzene to water. Journal of the American Chemical Society. 126: 10035-43. PMID 15303878 DOI: 10.1021/Ja0486972 |
0.569 |
|
2004 |
Mukhopadhyay P, Bharadwaj PK, Krishnan A, Das PK. Modulation of SHG responses via supramolecular association/dissociation between two complementary cryptands Journal of Organometallic Chemistry. 689: 4877-4881. DOI: 10.1016/J.Jorganchem.2004.06.061 |
0.526 |
|
2003 |
Mukhopadhyay P, Sarkar B, Bharadwaj PK, Nättinen K, Rissanen K. Metal binding characteristics of a laterally nonsymmetric aza cryptand upon functionalization with a pi-acceptor group. Inorganic Chemistry. 42: 4955-60. PMID 12895120 DOI: 10.1021/Ic034183C |
0.516 |
|
2003 |
Sarkar B, Mukhopadhyay P, Bharadwaj PK. Laterally non-symmetric aza-cryptands: synthesis, catalysis and derivatization to new receptors Coordination Chemistry Reviews. 236: 1-13. DOI: 10.1016/S0010-8545(02)00058-9 |
0.511 |
|
2002 |
Mukhopadhyay P, Bharadwaj PK, Krishnan A, Das PK. Synthesis and characterization of mono- and bis-D–π–A cryptand derivatives for second-order nonlinear optics and its modulation with different metal ion inputs J. Mater. Chem.. 12: 2786-2791. DOI: 10.1039/B203199J |
0.521 |
|
2002 |
Mukhopadhyay P, Bharadwaj PK, Savitha G, Krishnan A, Das PK. A new class of three dimensional D–π–A trigonal cryptand derivatives for second-order nonlinear optics J. Mater. Chem.. 12: 2237-2244. DOI: 10.1039/B202770B |
0.521 |
|
2000 |
Mukhopadhyay P, Bharadwaj PK, Savitha G, Krishnan A, Das PK. The first D–π–A octupolar cryptand molecule to exhibit bulk non-linearity Chemical Communications. 1815-1816. DOI: 10.1039/B004679P |
0.511 |
|
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