Year |
Citation |
Score |
2023 |
Gupta PK, Khan F, Misra R. NIR-Absorbing 1,1,4,4-Tetracyanobuta-1,3-diene- and Dicyanoquinodimethane-Functionalized Donor-Acceptor Phenothiazine Derivatives: Synthesis and Characterization. The Journal of Organic Chemistry. PMID 37820059 DOI: 10.1021/acs.joc.3c01029 |
0.84 |
|
2023 |
Sekaran B, Guragain M, Misra R, D'Souza F. β-Pyrrole Functionalized Push or Pull Porphyrins: Excited Charge Transfer Promoted Singlet Oxygen Generation. The Journal of Physical Chemistry. A. 127: 7964-7975. PMID 37707534 DOI: 10.1021/acs.jpca.3c05292 |
0.505 |
|
2023 |
Guragain M, Pinjari D, Misra R, D'Souza F. Zinc Tetrapyrrole Coordinated to Imidazole Functionalized Tetracyanobutadiene or Cyclohexa-2,5-diene-1,4-diylidene-expanded-tetracyanobutadiene Conjugates: Dark vs. Light-Induced Electron Transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). e202302665. PMID 37704573 DOI: 10.1002/chem.202302665 |
0.792 |
|
2023 |
Alsaleh AZ, Pinjari D, Misra R, D'Souza F. Far-Red Excitation Induced Electron Transfer in Bis Donor-AzaBODIPY Push-Pull Systems; Role of Nitrogenous Donors in Promoting Charge Separation. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301659. PMID 37401835 DOI: 10.1002/chem.202301659 |
0.794 |
|
2023 |
Jang Y, Sekaran B, Singh PP, Misra R, D'Souza F. Accelerated Intramolecular Charge Transfer in Tetracyanobutadiene- and Expanded Tetracyanobutadiene-Incorporated Asymmetric Triphenylamine-Quinoxaline Push-Pull Conjugates. The Journal of Physical Chemistry. A. PMID 37192382 DOI: 10.1021/acs.jpca.3c01732 |
0.533 |
|
2023 |
Sheokand M, Ji Tiwari N, Misra R. Near-IR absorbing 1,1,4,4-tetracyanobutadiene-functionalized phenothiazine sulfones. Organic & Biomolecular Chemistry. 21: 3896-3905. PMID 37165921 DOI: 10.1039/d3ob00361b |
0.334 |
|
2023 |
Popli C, Jang Y, Misra R, D'Souza F. Charge Resonance and Photoinduced Charge Transfer in Bis(,-dimethylaminophenyl-tetracyanobutadiene)-diketopyrrolopyrrole Multimodular System. The Journal of Physical Chemistry. B. 127: 4286-4299. PMID 37133351 DOI: 10.1021/acs.jpcb.3c01528 |
0.806 |
|
2023 |
Sheokand M, Alsaleh AZ, D'Souza F, Misra R. Excitation Wavelength-Dependent Charge Stabilization in Highly Interacting Phenothiazine Sulfone-Derived Donor-Acceptor Constructs. The Journal of Physical Chemistry. B. PMID 36938962 DOI: 10.1021/acs.jpcb.2c08472 |
0.554 |
|
2023 |
Bianconi T, Cesaretti A, Mancini P, Montegiove N, Calzoni E, Ekbote A, Misra R, Carlotti B. Room-Temperature Phosphorescence and Cellular Phototoxicity Activated by Triplet Dynamics in Aggregates of Push-Pull Phenothiazine-Based Isomers. The Journal of Physical Chemistry. B. 127: 1385-1398. PMID 36735941 DOI: 10.1021/acs.jpcb.2c07717 |
0.737 |
|
2022 |
Patil Y, Butenschön H, Misra R. Tetracyanobutadiene Bridged Push-Pull Chromophores: Development of New Generation Optoelectronic Materials. Chemical Record (New York, N.Y.). e202200208. PMID 36202630 DOI: 10.1002/tcr.202200208 |
0.715 |
|
2022 |
Yadav IS, Jang Y, Rout Y, Thomas MB, Misra R, D'Souza F. Near-IR Intramolecular Charge Transfer in Strongly Interacting Diphenothiazene-TCBD and Diphenothiazene-DCNQ Push-Pull Triads. Chemistry (Weinheim An Der Bergstrasse, Germany). e202200348. PMID 35275434 DOI: 10.1002/chem.202200348 |
0.826 |
|
2022 |
Huang P, Kazim S, Lezama L, Misra R, Ahmad S. Leverage of Pyridine Isomer on Phenothiazine Core: Organic Semiconductors as Selective Layers in Perovskite Solar Cells. Acs Applied Materials & Interfaces. 14: 5729-5739. PMID 35061363 DOI: 10.1021/acsami.1c21996 |
0.373 |
|
2021 |
D'Souza F, Misra R, Bijesh S, Dawson A, Jang Y, MohanSingh KV. Charge-Transfer in Panchromatic Porphyrin-Tetracyanobuta-1,3-diene-Donor Conjugates: Switching the Role of Porphyrin in the Charge Separation Process. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34375474 DOI: 10.1002/chem.202102865 |
0.605 |
|
2021 |
D'Souza F, Khan F, Jang Y, Patil Y, Misra R. Photoinduced Charge Separation Prompted Intervalence Charge Transfer in a Bis(thienyl)diketopyrrolopyrrole Bridged Donor-TCBD Push-Pull System. Angewandte Chemie (International Ed. in English). PMID 34258866 DOI: 10.1002/anie.202108293 |
0.817 |
|
2021 |
Huang P, Manju, Kazim S, Lezama L, Misra R, Ahmad S. Tailoring of a Phenothiazine Core for Electrical Conductivity and Thermal Stability: Hole-Selective Layers in Perovskite Solar Cells. Acs Applied Materials & Interfaces. PMID 34231361 DOI: 10.1021/acsami.1c08470 |
0.337 |
|
2021 |
Rout Y, Montanari C, Pasciucco E, Misra R, Carlotti B. Tuning the Fluorescence and the Intramolecular Charge Transfer of Phenothiazine Dipolar and Quadrupolar Derivatives by Oxygen Functionalization. Journal of the American Chemical Society. PMID 34161725 DOI: 10.1021/jacs.1c04173 |
0.829 |
|
2021 |
Jang Y, Rout Y, Misra R, D'Souza F. Symmetric and Asymmetric Push-Pull Conjugates: Significance of Pull Group Strength on Charge Transfer and Separation. The Journal of Physical Chemistry. B. 125: 4067-4075. PMID 33872029 DOI: 10.1021/acs.jpcb.0c09996 |
0.816 |
|
2021 |
Khan F, Ekbote A, Mobin SM, Misra R. Mechanochromism and Aggregation-Induced Emission in Phenanthroimidazole Derivatives: Role of Positional Change of Different Donors in a Multichromophoric Assembly. The Journal of Organic Chemistry. PMID 33399462 DOI: 10.1021/acs.joc.0c02404 |
0.823 |
|
2020 |
Yadav IS, Alsaleh AZ, Misra R, D'Souza F. Charge stabilization electron exchange: excited charge separation in symmetric, central triphenylamine derived, dimethylaminophenyl-tetracyanobutadiene donor-acceptor conjugates. Chemical Science. 12: 1109-1120. PMID 34163878 DOI: 10.1039/d0sc04648e |
0.787 |
|
2020 |
D'Souza F, Pinjari D, Alsaleh A, Patil Y, Misra R. Interfacing High-Energy Charge Transfer States to a Near-IR Sensitizer for Efficient Electron Transfer upon Near-IR Irradiation. Angewandte Chemie (International Ed. in English). PMID 33027554 DOI: 10.1002/anie.202013036 |
0.797 |
|
2020 |
D'Souza F, Popli C, Jang Y, Patil Y, Misra R. Formation of Highly Efficient, Long-Lived Charge Separated States in Star-Shaped Ferrocene-Diketopyrrolopyrrole-Triphenylamine Donor-Acceptor-Donor Conjugates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32589288 DOI: 10.1002/Chem.202002851 |
0.821 |
|
2020 |
Lee DY, Sivakumar G, Manju M, Misra R, Seok SI. Carbazole-based spiro[fluorene-9,9'-xanthene] as efficient hole-transporting material for perovskite solar cells. Acs Applied Materials & Interfaces. PMID 32476415 DOI: 10.1021/Acsami.0C06318 |
0.411 |
|
2020 |
Huang P, Manju, Kazim S, Sivakumar G, Salado M, Misra R, Ahmad S. Pyridine Bridging Diphenylamine-Carbazole with Linking Topology as Rational Hole Transporter for Perovskite Solar Cells Fabrication. Acs Applied Materials & Interfaces. PMID 32383376 DOI: 10.1021/Acsami.0C03584 |
0.427 |
|
2020 |
Poddar M, Jang Y, Misra R, D'Souza F. Excited State Electron Transfer in 1,1,4,4-Tetracyanobuta-1,3-Diene (TCBD)- and Cyclohexa-2,5-Diene-1,4-Diylidene-Expanded TCBD-Substituted BODIPY-Phenothiazines Donor-Acceptor Conjugates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32160356 DOI: 10.1002/Chem.202000346 |
0.78 |
|
2020 |
Rout Y, Chauhan V, Misra R. Synthesis and characterization of isoindigo-based push-pull chromophores. The Journal of Organic Chemistry. PMID 32126766 DOI: 10.1021/Acs.Joc.9B03267 |
0.835 |
|
2020 |
Khan F, Urbonas E, Volyniuk D, Grazulevicius JV, Mobin SM, Misra R. White hyperelectrofluorescence from solution-processable OLEDs based on phenothiazine substituted tetraphenylethylene derivatives Journal of Materials Chemistry C. 8: 13375-13388. DOI: 10.1039/D0Tc03136D |
0.786 |
|
2020 |
Ekbote A, Mobin SM, Misra R. Stimuli-responsive phenothiazine-based donor–acceptor isomers: AIE, mechanochromism and polymorphism Journal of Materials Chemistry C. 8: 3589-3602. DOI: 10.1039/C9Tc05192A |
0.735 |
|
2020 |
Chaudhary A, Poddar M, Pathak DK, Misra R, Kumar R. Electron Donor Ferrocenyl Phenothiazine: Counter Ion for Improving All-Organic Electrochromism Acs Applied Electronic Materials. 2: 2994-3000. DOI: 10.1021/acsaelm.0c00606 |
0.602 |
|
2020 |
Rout Y, Cesaretti A, Ferraguzzi E, Carlotti B, Misra R. Multiple Intramolecular Charge Transfers in Multimodular Donor–Acceptor Chromophores with Large Two-Photon Absorption The Journal of Physical Chemistry C. 124: 24631-24643. DOI: 10.1021/acs.jpcc.0c07616 |
0.806 |
|
2020 |
Poddar M, Cesaretti A, Ferraguzzi E, Carlotti B, Misra R. Singlet and Triplet Excited-State Dynamics of 3,7-Bis(arylethynyl)phenothiazines: Intramolecular Charge Transfer and Reverse Intersystem Crossing The Journal of Physical Chemistry C. 124: 17864-17878. DOI: 10.1021/Acs.Jpcc.0C01786 |
0.717 |
|
2020 |
Rout Y, Chauhan V, Misra R. Synthesis and Characterizationof Isoindigo-BasedPush–Pull Chromophores Journal of Organic Chemistry. DOI: 10.1021/Acs.Joc.9B03267.S001 |
0.832 |
|
2020 |
Poddar M, Misra R. Recent advances of BODIPY based derivatives for optoelectronic applications Coordination Chemistry Reviews. 421: 213462. DOI: 10.1016/J.Ccr.2020.213462 |
0.708 |
|
2020 |
Pinjari D, Alsaleh AZ, Patil Y, Misra R, D'Souza F. Cover Picture: Interfacing High‐Energy Charge‐Transfer States to a Near‐IR Sensitizer for Efficient Electron Transfer upon Near‐IR Irradiation (Angew. Chem. Int. Ed. 52/2020) Angewandte Chemie International Edition. 59: 23345-23345. DOI: 10.1002/anie.202014552 |
0.8 |
|
2020 |
Pinjari D, Alsaleh AZ, Patil Y, Misra R, D'Souza F. Titelbild: Interfacing High‐Energy Charge‐Transfer States to a Near‐IR Sensitizer for Efficient Electron Transfer upon Near‐IR Irradiation (Angew. Chem. 52/2020) Angewandte Chemie. 132: 23549-23549. DOI: 10.1002/ange.202014552 |
0.8 |
|
2019 |
Patil Y, Misra R. Metal Functionalized Diketopyrrolopyrroles: A Promising Class of Materials for Optoelectronic Applications. Chemical Record (New York, N.Y.). PMID 31833617 DOI: 10.1002/Tcr.201900061 |
0.715 |
|
2019 |
D'Souza F, Bijesh S, Jang Y, Misra R. Push-Pull Porphyrins via β -Pyrrole Functionalization: Evidence of Excited State Events Leading to High-Potential Charge-Separated States. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31415117 DOI: 10.1002/Chem.201902286 |
0.616 |
|
2019 |
Sharma R, Thomas M, Misra R, D'Souza F. Strong Ground and Excited State Charge Transfer in C3-Symmetric Truxene Derived, Low-Band Gap, Phenothiazine-Tetracyanobutadine (TCBD) and Expanded TCBD Conjugates. Angewandte Chemie (International Ed. in English). PMID 30710495 DOI: 10.1002/Anie.201814388 |
0.767 |
|
2019 |
Patil Y, Misra R. Rational molecular design towards NIR absorption: efficient diketopyrrolopyrrole derivatives for organic solar cells and photothermal therapy Journal of Materials Chemistry C. 7: 13020-13031. DOI: 10.1039/C9Tc03640G |
0.719 |
|
2019 |
Poddar M, Sivakumar G, Misra R. Donor–acceptor substituted 1,8-naphthalimides: design, synthesis, and structure–property relationship Journal of Materials Chemistry C. 7: 14798-14815. DOI: 10.1039/C9Tc02634G |
0.682 |
|
2019 |
Khan F, Ekbote A, Misra R. Reversible mechanochromism and aggregation induced enhanced emission in phenothiazine substituted tetraphenylethylene New Journal of Chemistry. 43: 16156-16163. DOI: 10.1039/C9Nj03290H |
0.785 |
|
2019 |
Rout Y, Mobin SM, Misra R. Tetracyanobutadiene (TCBD) functionalized benzothiadiazole derivatives: effect of donor strength on the [2+2] cycloaddition–retroelectrocyclization reaction New Journal of Chemistry. 43: 12299-12307. DOI: 10.1039/C9Nj01887E |
0.804 |
|
2019 |
Rout Y, Jang Y, Gobeze HB, Misra R, D’Souza F. Conversion of Large-Bandgap Triphenylamine–Benzothiadiazole to Low-Bandgap, Wide-Band Capturing Donor–Acceptor Systems by Tetracyanobutadiene and/or Dicyanoquinodimethane Insertion for Ultrafast Charge Separation The Journal of Physical Chemistry C. 123: 23382-23389. DOI: 10.1021/Acs.Jpcc.9B06632 |
0.796 |
|
2019 |
Carlotti B, Poddar M, Elisei F, Spalletti A, Misra R. Energy-Transfer and Charge-Transfer Dynamics in Highly Fluorescent Naphthalimide–BODIPY Dyads: Effect of BODIPY Orientation The Journal of Physical Chemistry C. 123: 24362-24374. DOI: 10.1021/Acs.Jpcc.9B05851 |
0.689 |
|
2019 |
Sharma R, Thomas MB, Misra R, D'Souza F. Strong Ground‐ and Excited‐State Charge Transfer in
C
3
‐Symmetric Truxene‐Derived Phenothiazine‐Tetracyanobutadine and Expanded Conjugates Angewandte Chemie. 131: 4394-4399. DOI: 10.1002/ange.201814388 |
0.685 |
|
2018 |
Misra R. 1,8-Naphthalimide Substituted BODIPY Dyads: Synthesis, Structure, Properties and Live-Cell Imaging. Chemistry, An Asian Journal. PMID 30011132 DOI: 10.1002/Asia.201800816 |
0.496 |
|
2018 |
Patil Y, Misra R. Small Molecule Based Non-fullerene Acceptors: A Comparative Study. Chemical Record (New York, N.Y.). PMID 29888443 DOI: 10.1002/Tcr.201800037 |
0.734 |
|
2018 |
Maragani R, Thomas M, Misra R, D'Souza F. C-Symmetric Positional Isomers of BODIPY Substituted Triazines: Synthesis and Excited State Properties. The Journal of Physical Chemistry. A. PMID 29733599 DOI: 10.1021/Acs.Jpca.8B02967 |
0.64 |
|
2018 |
Rout Y, Misra R, Singhal R, Biswas S, Sharma GD. Phenothiazine-based small-molecule organic solar cells with power conversion efficiency over 7% and open circuit voltage of about 1.0 V using solvent vapor annealing. Physical Chemistry Chemical Physics : Pccp. PMID 29435540 DOI: 10.1039/C7Cp08308D |
0.804 |
|
2018 |
Ekbote A, Mobin SM, Misra R. Structure–property relationship in multi-stimuli responsive D–A–A′ benzothiazole functionalized isomers Journal of Materials Chemistry C. 6: 10888-10901. DOI: 10.1039/C8Tc04310H |
0.733 |
|
2018 |
Gangala S, Misra R. Spiro-linked organic small molecules as hole-transport materials for perovskite solar cells Journal of Materials Chemistry A. 6: 18750-18765. DOI: 10.1039/C8Ta08503J |
0.376 |
|
2018 |
Ekbote A, Han SH, Jadhav T, Mobin SM, Lee JY, Misra R. Stimuli responsive AIE active positional isomers of phenanthroimidazole as non-doped emitters in OLEDs Journal of Materials Chemistry C. 6: 2077-2087. DOI: 10.1039/C7Tc05450E |
0.779 |
|
2018 |
Patil Y, Popli C, Misra R. Near-infrared absorbing tetracyanobutadiene-bridged diketopyrrolopyrroles New Journal of Chemistry. 42: 3892-3899. DOI: 10.1039/C7Nj05162J |
0.809 |
|
2018 |
Sharma R, Maragani R, Misra R. C3-Symmetric star shaped donor–acceptor truxenes: synthesis and photophysical, electrochemical and computational studies New Journal of Chemistry. 42: 882-890. DOI: 10.1039/C7Nj03934D |
0.672 |
|
2018 |
Seco CR, Vidal-Ferran A, Misra R, Sharma GD, Palomares E. Efficient Non-polymeric Heterojunctions in Ternary Organic Solar Cells Acs Applied Energy Materials. 1: 4203-4210. DOI: 10.1021/ACSAEM.8B00828 |
0.278 |
|
2018 |
Bucher L, Desbois N, Harvey PD, Gros CP, Misra R, Sharma GD. Nonfullerene Polymer Solar Cells Reaching a 9.29% Efficiency Using a BODIPY-Thiophene Backboned Donor Material Acs Applied Energy Materials. 1: 3359-3368. DOI: 10.1021/acsaem.8b00535 |
0.298 |
|
2018 |
Sharma R, Volyniuk D, Popli C, Bezvikonnyi O, Grazulevicius JV, Misra R. Strategy Toward Tuning Emission of Star-Shaped Tetraphenylethene-Substituted Truxenes for Sky-Blue and Greenish-White Organic Light-Emitting Diodes The Journal of Physical Chemistry C. 122: 15614-15624. DOI: 10.1021/Acs.Jpcc.8B00777 |
0.812 |
|
2018 |
Ansari MS, Maragani R, Banik A, Misra R, Qureshi M. Enhanced photovoltaic performance using biomass derived nano 3D ZnO hierarchical superstructures and a D−A type CS-Symmetric triphenylamine linked bisthiazole Electrochimica Acta. 259: 262-275. DOI: 10.1016/J.Electacta.2017.10.174 |
0.484 |
|
2018 |
Popli C, Patil Y, Misra R. Design and Synthesis of N
-Phenylcarbazole-Substituted Diketopyrrolopyrrole-Based Monomers and Dimers: A Comparative Study European Journal of Organic Chemistry. 2018: 6474-6481. DOI: 10.1002/Ejoc.201801072 |
0.787 |
|
2018 |
Bijesh S, Misra R. Triphenylamine Functionalized Unsymmetrical Quinoxalines Asian Journal of Organic Chemistry. 7: 1882-1892. DOI: 10.1002/Ajoc.201800384 |
0.331 |
|
2017 |
Maragani R, Ansari MS, Banik A, Misra R, Qureshi M. -Symmetric Triphenylamine-Linked Bisthiazole-Based Metal-Free Donor-Acceptor Organic Dye for Efficient ZnO Nanoparticles-Based Dye-Sensitized Solar Cells: Synthesis, Theoretical Studies, and Photovoltaic Properties. Acs Omega. 2: 5981-5991. PMID 31457851 DOI: 10.1021/acsomega.7b01100 |
0.455 |
|
2017 |
Misra R. Diketopyrrolopyrrole-based and tetracyano-bridged small molecules for bulk heterojunction organic solar cells. Chemistry, An Asian Journal. PMID 29219247 DOI: 10.1002/Asia.201701493 |
0.444 |
|
2017 |
Misra R, Poddar M. NIR Absorbing Donor-Acceptor Based 1,1,2,2-Tetracyanobutadiene (TCBD) and Cyclohexa-2,5-Diene-1,4-Ylidene-Expanded TCBD Substituted Ferrocenyl-Phenothiazines. Chemistry, An Asian Journal. PMID 28901716 DOI: 10.1002/Asia.201700879 |
0.682 |
|
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 |
0.831 |
|
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 |
0.817 |
|
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 |
0.757 |
|
2017 |
Maragani R, Misra R, Roy MS, Singh MK, Sharma GD. (D-π-A)2-π-D-A type ferrocenyl bisthiazole linked triphenylamine based molecular systems for DSSC: synthesis, experimental and theoretical performance studies. Physical Chemistry Chemical Physics : Pccp. PMID 28300259 DOI: 10.1039/C7Cp00612H |
0.472 |
|
2017 |
Patil Y, Misra R, Singh MK, Sharma GD. Ferrocene-diketopyrrolopyrrole based small molecule donors for bulk heterojunction solar cells. Physical Chemistry Chemical Physics : Pccp. PMID 28239736 DOI: 10.1039/C7Cp00231A |
0.76 |
|
2017 |
Jadhav T, Choi JM, Shinde J, Lee JY, Misra R. Mechanochromism and electroluminescence in positional isomers of tetraphenylethylene substituted phenanthroimidazoles Journal of Materials Chemistry C. 5: 6014-6020. DOI: 10.1039/C7Tc00950J |
0.704 |
|
2017 |
Patil Y, Misra R, Singhal R, Sharma GD. Ferrocene-diketopyrrolopyrrole based non-fullerene acceptors for bulk heterojunction polymer solar cells Journal of Materials Chemistry A. 5: 13625-13633. DOI: 10.1039/C7Ta03322B |
0.715 |
|
2017 |
Ekbote A, Jadhav T, Misra R. T-Shaped donor–acceptor–donor type tetraphenylethylene substituted quinoxaline derivatives: aggregation-induced emission and mechanochromism New Journal of Chemistry. 41: 9346-9353. DOI: 10.1039/C7Nj01531C |
0.798 |
|
2017 |
Patil Y, Misra R, Keshtov ML, Sharma GD. Small molecule carbazole-based diketopyrrolopyrroles with tetracyanobutadiene acceptor unit as a non-fullerene acceptor for bulk heterojunction organic solar cells Journal of Materials Chemistry A. 5: 3311-3319. DOI: 10.1039/C6Ta09607G |
0.733 |
|
2017 |
Misra R, Jadhav T, Nevonen D, Monzo EM, Mobin SM, Nemykin VN. Synthesis, Structures, and Redox Properties of Tetracyano-Bridged Diferrocene Donor–Acceptor–Donor Systems Organometallics. 36: 4490-4498. DOI: 10.1021/Acs.Organomet.7B00728 |
0.758 |
|
2017 |
Patil Y, Shinde J, Misra R. Near-infrared absorbing metal functionalized diketopyrrolopyrroles Journal of Organometallic Chemistry. 852: 48-53. DOI: 10.1016/J.Jorganchem.2017.10.014 |
0.744 |
|
2017 |
Patil Y, Misra R. Tetracyanobutadiene bridged ferrocene and triphenylamine functionalized pyrazabole dimers Journal of Organometallic Chemistry. 840: 23-29. DOI: 10.1016/J.Jorganchem.2017.03.048 |
0.789 |
|
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 |
0.805 |
|
2017 |
Maragani R, Sharma R, Misra R. Donor-Acceptor Triphenylvinyl and Tetraphenyl Conjugates: Synthesis, Aggregation and Computational Studies Chemistryselect. 2: 10033-10037. DOI: 10.1002/SLCT.201701373 |
0.618 |
|
2017 |
Patil Y, Jadhav T, Dhokale B, Butenschön H, Misra R. Donor Substituted Pyrazabole Monomers and Dimers: Design, Synthesis and Properties Chemistryselect. 2: 415-420. DOI: 10.1002/SLCT.201601704 |
0.815 |
|
2017 |
Maragani R, Bijesh S, Sharma R, Misra R. C
s
-Symmetric Donor-Acceptor Bis(thiazole)s: Synthesis and Photophysical, Electrochemical, and Computational Studies Asian Journal of Organic Chemistry. 6: 1408-1414. DOI: 10.1002/Ajoc.201700274 |
0.704 |
|
2016 |
Patil Y, Misra R, Chen FC, Sharma GD. Small molecule based N-phenyl carbazole substituted diketopyrrolopyrroles as donors for solution-processed bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics : Pccp. PMID 27489031 DOI: 10.1039/C6Cp03767D |
0.735 |
|
2016 |
Patil Y, Misra R, Sharma A, Sharma GD. D-A-D-π-D-A-D type diketopyrrolopyrrole based small molecule electron donors for bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics : Pccp. PMID 27292157 DOI: 10.1039/C6Cp02700H |
0.745 |
|
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 |
0.766 |
|
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 |
0.741 |
|
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 |
0.788 |
|
2016 |
Sheshashena Reddy T, Maragani R, Misra R. Triarylborane substituted naphthalimide as a fluoride and cyanide ion sensor. Dalton Transactions (Cambridge, England : 2003). 45: 2549-53. PMID 26727393 DOI: 10.1039/C5Dt04039F |
0.413 |
|
2016 |
Patil Y, Misra R, Chen FC, Keshtov ML, Sharma GD. Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells Rsc Advances. 6: 99685-99694. DOI: 10.1039/C6Ra10442H |
0.759 |
|
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 |
0.701 |
|
2016 |
Reddy TS, Maragani R, Dhokale B, Mobin SM, Misra R. Heteroatom-connected ferrocenyl substituted naphthalimides Rsc Advances. 6: 7746-7754. DOI: 10.1039/C5Ra26369G |
0.755 |
|
2016 |
Jadhav T, Dhokale B, Patil Y, Mobin SM, Misra R. Multi-Stimuli Responsive Donor–Acceptor Tetraphenylethylene Substituted Benzothiadiazoles The Journal of Physical Chemistry C. 120: 24030-24040. DOI: 10.1021/Acs.Jpcc.6B09015 |
0.809 |
|
2016 |
Jadhav T, Choi JM, Dhokale B, Mobin SM, Lee JY, Misra R. Effect of End Groups on Mechanochromism and Electroluminescence in Tetraphenylethylene Substituted Phenanthroimidazoles The Journal of Physical Chemistry C. 120: 18487-18495. DOI: 10.1021/Acs.Jpcc.6B06277 |
0.825 |
|
2016 |
Patil Y, Misra R, Keshtov ML, Sharma GD. 1,1,4,4-Tetracyanobuta-1,3-diene Substituted Diketopyrrolopyrroles: An Acceptor for Solution Processable Organic Bulk Heterojunction Solar Cells Journal of Physical Chemistry C. 120: 6324-6335. DOI: 10.1021/Acs.Jpcc.5B12307 |
0.754 |
|
2016 |
Maragani R, Reddy TS, Misra R. C S -symmetric triarylborane substituted bisthiazole for selective detection of F − and CN − ions Tetrahedron Letters. 57: 3853-3857. DOI: 10.1016/J.Tetlet.2016.07.051 |
0.402 |
|
2016 |
Jadhav T, Choi JM, Lee JY, Dhokale B, Misra R. Non-doped blue organic light emitting devices based on tetraphenylethylene-π-imidazole derivatives Organic Electronics: Physics, Materials, Applications. 37: 448-452. DOI: 10.1016/J.Orgel.2016.07.009 |
0.811 |
|
2016 |
Sharma R, Maragani R, Misra R. Ferrocenyl aza-dipyrromethene and aza-BODIPY: Synthesis and properties Journal of Organometallic Chemistry. 825: 8-14. DOI: 10.1016/J.Jorganchem.2016.10.019 |
0.733 |
|
2016 |
Dhokale B, Jadhav T, Patil Y, Misra R. Symmetrical and unsymmetrical ferrocenyl perylenediimides: Design, synthesis and properties Dyes and Pigments. 134: 164-170. DOI: 10.1016/J.Dyepig.2016.07.006 |
0.842 |
|
2016 |
Misra R, Maragani R, Arora D, Sharma A, Sharma GD. Positional isomers of pyridine linked triphenylamine-based donor-acceptor organic dyes for efficient dye-sensitized solar cells Dyes and Pigments. 126: 38-45. DOI: 10.1016/J.Dyepig.2015.11.008 |
0.483 |
|
2016 |
Misra R, Maragani R, Singh CP, Chari R. Photonic properties of star shaped ferrocenyl substituted triazines Dyes and Pigments. 126: 110-117. DOI: 10.1016/J.Dyepig.2015.10.011 |
0.435 |
|
2016 |
Singh S, Reddy TS, Panwar R, Misra R, Pratap R. 2-(2,2-Bis-benzylamino-1-cyano-vinyl)-benzonitrile: A Selective Turn-off Fluorescent Cu2+Sensor Chemistryselect. 1: 2576-2580. DOI: 10.1002/SLCT.201600504 |
0.231 |
|
2016 |
Patil Y, Jadhav T, Dhokale B, Misra R. Design and Synthesis of Low HOMO-LUMO GapN-Phenylcarbazole-Substituted Diketopyrrolopyrroles Asian Journal of Organic Chemistry. 5: 1008-1014. DOI: 10.1002/Ajoc.201600194 |
0.79 |
|
2015 |
Dhokale B, Jadhav T, Mobin SM, Misra R. Tetracyanobutadiene functionalized ferrocenyl BODIPY dyes. Dalton Transactions (Cambridge, England : 2003). PMID 26675115 DOI: 10.1039/C5Dt04037J |
0.808 |
|
2015 |
Jadhav T, Misra R, Biswas S, Sharma GD. Bulk heterojunction organic solar cells based on carbazole-BODIPY conjugate small molecules as donors with high open circuit voltage. Physical Chemistry Chemical Physics : Pccp. 17: 26580-8. PMID 26394373 DOI: 10.1039/C5Cp04807A |
0.733 |
|
2015 |
Misra R, Jadhav T, Dhokale B, Mobin SM. Colorimetric and fluorimetric detection of fluoride and cyanide ions using tri and tetra coordinated boron containing chromophores. Dalton Transactions (Cambridge, England : 2003). 44: 16052-60. PMID 26285867 DOI: 10.1039/C5Dt02356D |
0.796 |
|
2015 |
Dhokale B, Jadhav T, Mobin SM, Misra R. Meso Alkynylated Tetraphenylethylene (TPE) and 2,3,3-Triphenylacrylonitrile (TPAN) Substituted BODIPYs. The Journal of Organic Chemistry. 80: 8018-25. PMID 26191612 DOI: 10.1021/Acs.Joc.5B01117 |
0.832 |
|
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 |
0.756 |
|
2015 |
Dhokale B, Jadhav T, Mobin SM, Misra R. Meso enyne substituted BODIPYs: synthesis, structure and properties. Dalton Transactions (Cambridge, England : 2003). 44: 15803-12. PMID 25812138 DOI: 10.1039/C5Dt00565E |
0.816 |
|
2015 |
Jadhav T, Dhokale B, Mobin SM, Misra R. Aggregation induced emission and mechanochromism in pyrenoimidazoles Journal of Materials Chemistry C. 3: 9981-9988. DOI: 10.1039/C5Tc02181B |
0.811 |
|
2015 |
Jadhav T, Dhokale B, Misra R. Effect of the cyano group on solid state photophysical behavior of tetraphenylethene substituted benzothiadiazoles Journal of Materials Chemistry C. 3: 9063-9068. DOI: 10.1039/C5Tc01871D |
0.816 |
|
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 |
0.769 |
|
2015 |
Jadhav T, Dhokale B, Patil Y, Misra R. Aggregation induced emission and mechanochromism in tetraphenylethene substituted pyrazabole Rsc Advances. 5: 68187-68191. DOI: 10.1039/C5Ra12697E |
0.81 |
|
2015 |
Dhokale B, Jadhav T, Mobin SM, Misra R. Synergistic effect of donors on tetracyanobutadine (TCBD) substituted ferrocenyl pyrenes Rsc Advances. 5: 57692-57699. DOI: 10.1039/C5Ra11433K |
0.833 |
|
2015 |
Jadhav T, Dhokale B, Mobin SM, Misra R. Mechanochromism and aggregation induced emission in benzothiazole substituted tetraphenylethylenes: A structure function correlation Rsc Advances. 5: 29878-29884. DOI: 10.1039/C5Ra04881H |
0.828 |
|
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 |
0.802 |
|
2015 |
Gautam P, Maragani R, Misra R. Aryl-substituted symmetrical and unsymmetrical benzothiadiazoles Rsc Advances. 5: 18288-18294. DOI: 10.1039/C4Ra15424J |
0.77 |
|
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 |
0.788 |
|
2015 |
Sharma GD, Angaridis PA, Pipou S, Zervaki GE, Nikolaou V, Misra R, Coutsolelos AG. Efficient co-sensitization of dye-sensitized solar cells by novel porphyrin/triazine dye and tertiary aryl-amine organic dye Organic Electronics: Physics, Materials, Applications. 25: 295-307. DOI: 10.1016/J.Orgel.2015.06.048 |
0.488 |
|
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 |
0.762 |
|
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 |
0.736 |
|
2015 |
Patil Y, Jadhav T, Dhokale B, Misra R. Tuning of the HOMO-LUMO Gap of Symmetrical and Unsymmetrical Ferrocenyl-Substituted Diketopyrrolopyrroles European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201501123 |
0.83 |
|
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 |
0.829 |
|
2014 |
Dhokale B, Jadhav T, Mobin SM, Misra R. Meso enamine substituted BODIPYs. Chemical Communications (Cambridge, England). 50: 9119-21. PMID 24985933 DOI: 10.1039/C4Cc03857F |
0.79 |
|
2014 |
Misra R, Jadhav T, Dhokale B, Mobin SM. Reversible mechanochromism and enhanced AIE in tetraphenylethene substituted phenanthroimidazoles. Chemical Communications (Cambridge, England). 50: 9076-8. PMID 24983656 DOI: 10.1039/C4Cc02824D |
0.812 |
|
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 |
0.759 |
|
2014 |
Misra R, Sharma R, Mobin SM. Star shaped ferrocenyl truxenes: synthesis, structure and properties. Dalton Transactions (Cambridge, England : 2003). 43: 6891-6. PMID 24658688 DOI: 10.1039/C4Dt00210E |
0.713 |
|
2014 |
Misra R, Dhokale B, Jadhav T, Mobin SM. The quenching of fluorescence as an indicator of donor-strength in meso arylethynyl BODIPYs. Dalton Transactions (Cambridge, England : 2003). 43: 4854-61. PMID 24481177 DOI: 10.1039/C3Dt53056F |
0.833 |
|
2014 |
Misra R, Jadhav T, Mobin SM. Ferrocenyl pyrazaboles: design, synthesis, structure, and properties. Dalton Transactions (Cambridge, England : 2003). 43: 2013-22. PMID 24270929 DOI: 10.1039/C3Dt52315B |
0.776 |
|
2014 |
Sahu SN, Gupta MK, Jadhav T, Yadav P, Singh S, Misra R, Pratap R. Substituent dependent tunable fluorescence in thieno[3,2-c]pyrans Rsc Advances. 4: 56779-56783. DOI: 10.1039/C4Ra11337C |
0.736 |
|
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 |
0.759 |
|
2014 |
Misra R, Maragani R, Patel KR, Sharma GD. Synthesis, optical and electrochemical properties of new ferrocenyl substituted triphenylamine based donor-acceptor dyes for dye sensitized solar cells Rsc Advances. 4: 34904-34911. DOI: 10.1039/C4Ra03088E |
0.467 |
|
2014 |
Misra R, Dhokale B, Jadhav T, Mobin SM. Meso-Aryloxy and meso-arylaza linked BODIPY dimers: Synthesis, structures and properties New Journal of Chemistry. 38: 3579-3585. DOI: 10.1039/C4Nj00354C |
0.806 |
|
2014 |
Misra R, Maragani R, Jadhav T, Mobin SM. Ferrocenyl end capped molecular rods: Synthesis, structure, and properties New Journal of Chemistry. 38: 1446-1457. DOI: 10.1039/C3Nj01244A |
0.76 |
|
2014 |
Misra R, Dhokale B, Jadhav T, Mobin SM. Heteroatom-connected ferrocenyl BODIPYs: Synthesis, structure, and properties Organometallics. 33: 1867-1877. DOI: 10.1021/Om5002292 |
0.816 |
|
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 |
0.774 |
|
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 |
0.794 |
|
2014 |
Maragani R, Misra R. Ferrocenyl substituted triphenylamine based donor–acceptor molecular systems; synthesis, photophysical, electrochemical, and theoretical studies Tetrahedron. 70: 3390-3399. DOI: 10.1016/J.Tet.2014.03.096 |
0.537 |
|
2014 |
Sharma GD, Patel KR, Roy MS, Misra R. Characterization of two new (A-π)2-D-A type dyes with different central D unit and their application for dye sensitized solar cells Organic Electronics: Physics, Materials, Applications. 15: 1780-1790. DOI: 10.1016/J.Orgel.2014.05.002 |
0.464 |
|
2014 |
Singh CP, Sharma R, Shukla V, Khundrakpam P, Misra R, Bindra KS, Chari R. Optical limiting and nonlinear optical studies of ferrocenyl substituted calixarenes Chemical Physics Letters. 616: 189-195. DOI: 10.1016/J.Cplett.2014.10.030 |
0.612 |
|
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 |
0.771 |
|
2013 |
Misra R, Jadhav T, Mobin SM. Aryl pyrazaboles: a new class of tunable and highly fluorescent materials. Dalton Transactions (Cambridge, England : 2003). 42: 16614-20. PMID 24071967 DOI: 10.1039/C3Dt52154K |
0.763 |
|
2013 |
Misra R, Dhokale B, Jadhav T, Mobin SM. Donor-acceptor meso-alkynylated ferrocenyl BODIPYs: synthesis, structure, and properties. Dalton Transactions (Cambridge, England : 2003). 42: 13658-66. PMID 23903804 DOI: 10.1039/C3Dt51374B |
0.838 |
|
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 |
0.832 |
|
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 |
0.827 |
|
2013 |
Jadhav T, Maragani R, Misra R, Sreeramulu V, Rao DN, Mobin SM. Design and synthesis of donor-acceptor pyrazabole derivatives for multiphoton absorption. Dalton Transactions (Cambridge, England : 2003). 42: 4340-2. PMID 23396416 DOI: 10.1039/C3Dt33065F |
0.772 |
|
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 |
0.825 |
|
2013 |
Sharma R, Margani R, Mobin SM, Misra R. Ferrocenyl substituted calixarenes: synthesis, structure and properties Rsc Advances. 3: 5785. DOI: 10.1039/C3Ra00146F |
0.723 |
|
2013 |
Maragani R, Jadhav T, Mobin SM, Misra R. C3 symmetric ferrocenyl triazines: Synthesis, structure, and properties Rsc Advances. 3: 2889-2892. DOI: 10.1039/C2Ra23153K |
0.748 |
|
2013 |
Maragani R, Misra R. Donor–acceptor ferrocenyl triazines: synthesis and properties Tetrahedron Letters. 54: 5399-5402. DOI: 10.1016/J.Tetlet.2013.07.119 |
0.546 |
|
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 |
0.815 |
|
2012 |
Gautam P, Dhokale B, Mobin SM, Misra R. Ferrocenyl BODIPYs: synthesis, structure and properties Rsc Advances. 2: 12105. DOI: 10.1039/C2Ra21964F |
0.822 |
|
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 |
0.825 |
|
2012 |
Maragani R, Jadhav T, Mobin SM, Misra R. Synthesis, structure, photophysical, and electrochemical properties of donor-acceptor ferrocenyl derivatives Tetrahedron. 68: 7302-7308. DOI: 10.1016/J.Tet.2012.06.094 |
0.782 |
|
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 |
0.783 |
|
2009 |
Zhan X, Tan Z, Zhou E, Li Y, Misra R, Grant A, Domercq B, Zhang X, An Z, Zhang X, Barlow S, Kippelen B, Marder SR. Copolymers of perylene diimide with dithienothiophene and dithienopyrrole as electron-transport materials for all-polymer solar cells and field-effect transistors Journal of Materials Chemistry. 19: 5794. DOI: 10.1039/B907163F |
0.667 |
|
2008 |
Yoon MC, Misra R, Yoon ZS, Kim KS, Lim JM, Chandrashekar TK, Kim D. Photophysical properties of core-modified expanded porphyrins: nature of aromaticity and enhancement of ring planarity. The Journal of Physical Chemistry. B. 112: 6900-5. PMID 18481890 DOI: 10.1021/Jp800748N |
0.766 |
|
2008 |
Misra R, Chandrashekar TK. Structural diversity in expanded porphyrins. Accounts of Chemical Research. 41: 265-79. PMID 18281947 DOI: 10.1021/Ar700091K |
0.735 |
|
2007 |
Misra R, Kumar R, Chandrashekar TK, Joshi BS. 26pi aromatic core-modified hexaphyrins: syntheses, characterization, and structural diversities. The Journal of Organic Chemistry. 72: 1153-60. PMID 17288370 DOI: 10.1021/Jo061861E |
0.735 |
|
2007 |
Kumar R, Misra R, Chandrashekar TK, Suresh E. Near IR absorbing planar aromatic [34]octaphyrins(1.1.0.1.1.0.0.0) containing a quaterthiophene subunit. Chemical Communications (Cambridge, England). 43-5. PMID 17279255 DOI: 10.1039/B614290G |
0.711 |
|
2007 |
Kumar R, Misra R, Chandrashekar TK, Nag A, Goswami D, Suresh E, Suresh CH. One-pot synthesis of core-modified rubyrin, octaphyrin, and dodecaphyrin: Characterization and nonlinear optical properties European Journal of Organic Chemistry. 4552-4562. DOI: 10.1002/Ejoc.200700466 |
0.749 |
|
2006 |
Misra R, Kumar R, Chandrashekar TK, Suresh CH, Nag A, Goswami D. 22pi smaragdyrin molecular conjugates with aromatic phenylacetylenes and ferrocenes: Syntheses, electrochemical, and photonic properties. Journal of the American Chemical Society. 128: 16083-91. PMID 17165761 DOI: 10.1021/Ja0628295 |
0.761 |
|
2006 |
Misra R, Kumar R, Chandrashekar TK, Suresh CH. Meso-meso linked core modified 22π smaragdyrins with unusual absorption properties Chemical Communications. 4584-4586. PMID 17082850 DOI: 10.1039/B610578E |
0.75 |
|
2006 |
Kumar R, Misra R, Chandrashekar TK. Effect of meso aryl substituents on the synthesis of core-modified expanded porphyrins. Organic Letters. 8: 4847-50. PMID 17020318 DOI: 10.1021/Ol0619011 |
0.746 |
|
2006 |
Misra R, Kumar R, Chandrashekar TK, Nag A, Goswami D. Modified (22pi) smaragdyrins with large two-photon absorption cross section: a structure function correlation. Organic Letters. 8: 629-31. PMID 16468728 DOI: 10.1021/Ol052809S |
0.709 |
|
2005 |
Kumar R, Misra R, PrabhuRaja V, Chandrashekar TK. Modified expanded corrole-ferrocene conjugates: syntheses, structure and properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 5695-707. PMID 16034997 DOI: 10.1002/Chem.200500109 |
0.75 |
|
2005 |
Chandrashekar TK, Venkatraman S, Prabhuraja V, Misra R, Baskar V. Supramolecular Assemblies of Sulfur- and Selenium- Containing Expanded Porphyrins Mediated Through Noncovalent Interactions Phosphorus, Sulfur, and Silicon and the Related Elements. 180: 845-872. DOI: 10.1080/10426500590906364 |
0.702 |
|
2005 |
Misra R, Kumar R, PrabhuRaja V, Chandrashekar TK. Modified push–pull expanded corroles: Syntheses, structure and nonlinear optical properties Journal of Photochemistry and Photobiology a: Chemistry. 175: 108-117. DOI: 10.1016/J.Jphotochem.2005.04.024 |
0.766 |
|
2005 |
Misra R, Anand VG, Rath H, Chandrashekar TK. Core-modified octaphyrins: Syntheses and anion-binding properties Journal of Chemical Sciences. 117: 99-103. DOI: 10.1007/BF03356102 |
0.699 |
|
2005 |
Misra R, Anand VG, Rath H, Chandrashekar TK. Core-Modified Octaphyrins: Syntheses and Anion-Binding Properties Cheminform. 36. DOI: 10.1007/Bf03356102 |
0.735 |
|
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