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Selected Publications

















 

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Indresh S. Yadav, Ajyal Z. Alsaleh, Rajneesh Misra*, Francis D’Souza*, Charge stabilization electron exchange: excited charge separation in symmetric, central triphenylamine derived, dimethylaminophenyl-tetracyanobutadiene donor-acceptor conjugates. Chemical Science, 2020, 12, 1109-1120.

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Yogajivan Rout, Anupama Ekbotea,  Rajneesh Misra, Recent development on the synthesis, properties and applications of luminescent oxidized phenothiazine derivatives, J. Mater. Chem. C, 2021,9, 7508-7531.

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Yogajivan Rout, Vivek Chauhan, Rajneesh Misra*, Synthesis and Characterization of Isoindigo-Based Push-Pull Chromophores, New J. Chem., 2021, DOI: 10.1021/acs.joc.9b03267.

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Faizal Khan, Anupama Ekbote, Shaikh M. Mobin, and Rajneesh Misra*, Mechanochromism and Aggregation-Induced Emission in Phenanthroimidazole Derivatives: Role of Positional Change of Different Donors in a Multichromophoric Assembly, J. Org. Chem., 2021, 86, 2, 1560–1574.

2023

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  • T Bianconi, A Cesaretti, P Mancini, N Montegiove, E Calzoni, A Ekbote, R Misra*, and B Carlotti*, Room-Temperature Phosphorescence and Cellular Phototoxicity Activated by Triplet Dynamics in Aggregates of Push–Pull Phenothiazine-Based Isomers, J. Phys. Chem. B 2023, 127, 1385-1398.

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  • F Khan, R Misra*, Recent advances in the development of phenothiazine and its fluorescent derivatives for optoelectronic applications, J. Mater. Chem. C, 2023, 11, 2786

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  • M Sheokand, AZ Alsaleh, F D’Souza*, and R Misra*, Excitation Wavelength-Dependent Charge Stabilization in Highly Interacting Phenothiazine Sulfone-Derived Donor−Acceptor Constructs, J. Phys. Chem. B 2023, 127, 2761-2773.​

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  • M Sheokand, NJ Tiwari and R Misra*, Near-IR absorbing 1,1,4,4-tetracyanobutadiene-functionalized phenothiazine sulfones, Org. Biomol. Chem., 2023, DOI: 10.1039/d3ob00361b.

2022

  • Manju, S Kazim, L Lezama, R Misra*, and S Ahmad*, Leverage of Pyridine Isomer on Phenothiazine Core: Organic Semiconductors as Selective Layers in Perovskite Solar Cells, ACS Appl. Mater. Interfaces, 2022, 14, 5729-5739.

 

  • B Sekaran, R Misra*, Beta-Pyrrole functionalized porphyrins: Synthesis, electronic properties, and applications in sensing and DSSC, Coord. Chem. Rev., 2022, 453, 214312.

 

  • M Poddar, Y Rout, R Misra*, Donor-Acceptor Based 1,8-Naphthalimide Substituted Phenothiazines: Tuning of HOMO-LUMO Gap, Asian J. Org. Chem., 2022, 11, DOI: https://doi.org/10.1002/ajoc.202100628

 

  • F Khan, Y Rout and R Misra*, Donor Functionalized bis(thienyl)diketopyrrolopyrroles: Photophysical and Electrochemical properties, ISRAPS Bulletin 2022

 

  • F Khan, A Ekbote, G Singh and R Misra*, Mechanochromic luminogens with hypsochromically shifted emission switching property: Recent advances and perspectives, J. Mater. Chem. C, 2022, 10, 5024-5064.

 

 

 

 

 

 

 

 

 

  • Y Patil, H Butenschön, R Misra*, Tetracyanobutadiene Bridged Push-Pull Chromophores: Development of New Generation Optoelectronic Materials, Chem. Rec., 2022, 23, e202200208.

 

  • F Khan, M Mahmoudi, D Volyniuk, JV Grazulevicius, R Misra*, Stimuli-Responsive Phenothiazine- S, S-dioxide-Based Nondoped OLEDs with Color-Changeable Electroluminescence, Journal of Physical Chemistry C, 2022, 126, 15573-15586.

2021

  • B Dhokale, IS Yadav, SM Mobin and R Misra*, Thioether linked meso functionalized BODIPY DYEmer, J. Porphyr. Phthalocyanines, 2021, 25, 428-435.

 

  • B Sekaran, A Dawson, Y Jang, KV MohanSingh, R Misra*, F D'Souza*, Charge-Transfer in Panchromatic Porphyrin-Tetracyanobuta-1,3-Diene-Donor Conjugates: Switching the Role of Porphyrin in the Charge Separation Process, Chem. Eur. J., 2021, 27, 14335-14344.

 

  • F Khan, Y Jang, Y Patil, R Misra*, F D'Souza*, Photoinduced Charge Separation Prompted Intervalence Charge Transfer in a Bis(thienyl)diketopyrrolopyrrole Bridged Donor‐TCBD Push‐Pull System, Angew. Chem. Int. Ed., 2021, 60, 20518-20527.

 

  • Y Rout and R Misra*, Design and synthesis of 1,8-naphthalimide functionalized benzothiadiazoles, New J. Chem., 2021, 5, 9838-9845.

 

  • Y Jang, Y Rout, R Misra*, and F D’Souza*, Symmetric and Asymmetric Push−Pull Conjugates: Significance of Pull Group Strength on Charge Transfer and Separation, J. Phys. Chem. B, 2021, 125, 4067-4075.

 

  • Y Rout, C Montanari, E Pasciucco, R Misra*, and B Carlotti*, Tuning the Fluorescence and the Intramolecular Charge Transfer of Phenothiazine Dipolar and Quadrupolar Derivatives by Oxygen Functionalization, J. Am. Chem. Soc., 2021, 143, 9933-9943.

 

  • IS Yadav, AZ Alsaleh, R Misra*, and F D'Souza*, Charge stabilization via electron exchange: excited charge separation in symmetric, central triphenylamine derived, dimethylaminophenyl– tetracyanobutadiene donor–acceptor conjugates, Chem. Sci. J., 2021, 12, 1109-1120.

 

  • F Khan, A Ekbote, SM Mobin and R Misra*, Mechanochromism and Aggregation Induced Emission (AIE) in Phenanthroimidazole Derivatives: Role of Positional Change of Different Donors in a Multichromophoric Assembly, J. Org. Chem., 2021, 86, 1560-1574.

 

  • A Ekbote, SM Mobin and R Misra*, Stimuli-responsive phenothiazine-based donor–acceptor isomers: AIE, mechanochromism and polymorphism, J. Mater. Chem. C, 2021, 8, 3589-3602.

 

  • A Chaudhary, G Sivakumar, DK Pathak, M Tanwar, R Misra*, and R Kumar*, Pentafluorophenyl substituted fulleropyrrolidine: a molecule enabling the most efficient flexible electrochromic device with fast switching, J. Mater. Chem. C, 2021, 9, 3462-3469.

 

  • P Huang, Manju, S Kazim, L Lezama, R Misra*, and S Ahmad*, Tailoring of a Phenothiazine Core for Electrical Conductivity and Thermal Stability: Hole-Selective Layers in Perovskite Solar Cells, ACS Appl. Mater. Interfaces, 2021, 13, 33311-33320.

 

  • Y Rout, A Ekbote and R Misra*, Recent development on the synthesis, properties and applications of luminescent oxidized phenothiazine derivatives, J. Mater. Chem. C, 2021, 9, 7508-7531.

 

  • J Shinde, MB Thomas, M Poddar, R Misra*, and F D’Souza*, Does Location of BF2-Chelated Dipyrromethene (BODIPY) Ring Functionalization Affect Spectral and Electron Transfer Properties? Studies on α-, β-, and Meso-Functionalized BODIPY-Derived Donor–Acceptor Dyads and Triads, J. Phys. Chem. C, 2021, 125, 23911-23921.

 

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2020

  • F Khan, E Urbonas, D Volyniuk, JV Grazulevicius, SM Mobin and R Misra*, White hyperelectrofluorescence from solution-processable OLEDs based on phenothiazine substituted tetraphenylethylene derivatives, J. Mater. Chem. C. 2020, 8, 13375-13388.

 

 

  • D Pinjari, AZ Alsaleh, Y Patil, R Misra*, F D'Souza*, Interfacing High-Energy Charge-Transfer States to a Near-IR Sensitizer for Efficient Electron Transfer upon Near-IR Irradiation, Angew. Chem. Int. Ed., 2020, 132, 23697-23705.

 

  • A Ekbote, SM Mobin and R Misra*, Stimuli-responsive phenothiazine-based donor-acceptor isomers: AIE, mechanochromism and Polymorphism, J. Mater. Chem. C, 2020, 8, 3589-3602.

 

  • P Huang, Manju, S Kazim, G Sivakumar, M Salado, R Misra*, S Ahmad*, Pyridine Bridging Diphenylamine-Carbazole with Linking Topology as Rational Hole Transporter for Perovskite Solar Cells Fabrication, ACS Appl. Mater. Interfaces, 2020, 20, 22881-22890.

 

  • M Poddar, A Cesaretti, E Ferraguzzi, B Carlotti* and R Misra*, Singlet and Triplet Excited-State Dynamics of 3,7-Bis(arylethynyl)phenothiazines: Intramolecular Charge Transfer and Reverse Intersystem Crossing, J. Phys. Chem. C, 2020, 124, 17864-17878.

 

  • A Chaudhary, M Poddar, DK Pathak, R Misra*, and R Kumar*, Electron Donor Ferrocenyl Phenothiazine: Counter Ion for Improving All-Organic Electrochromism, ACS Appl. Electron. Mater, 2020, 2, 2994-3000.

 

  • DY Lee, G Sivakumar, Manju, R Misra*, and S Il Seok*, Carbazole-Based Spiro[fluorene-9,9′-xanthene] as an Efficient Hole-Transporting Material for Perovskite Solar Cells, ACS Appl. Mater. Interfaces, 2020, 12, 28246-28252.

 

  • M Poddar, Y Jang,  R Misra*, and F D'Souza*, 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‐Phenothiazine Donor–Acceptor Conjugates, Chem. Eur. J., 2020, 26, 6869-6878.

 

  • F D'Souza, C Popli, Y Jang, Y Patil, R Misra*, Formation of Highly Efficient, Long‐Lived Charge Separated States in Star‐Shaped Ferrocene‐Diketopyrrolopyrrole‐Triphenylamine Donor‐Acceptor‐Donor Conjugates, Chem. Eur. J., 2020, 26,15109-15115.

 

  • M Poddar and R Misra*, Recent advances of BODIPY based derivatives for optoelectronic applications, Coord. Chem. Rev., 2020, 421, 213462.

2019

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  • R Sharma, M Thomas, R Misra*, F D'Souza, Strong Ground and  Excited State Charge Transfer in C3-Symmetric Truxene Derived, Low-Band Gap, Phenothiazine-Tetracyanobutadine (TCBD) and Expanded TCBD Conjugates, Angew. Chem. Int. Ed., 2019, 58, 4350-4355.

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  • F Khan, A Ekbote and R Misra*, Reversible mechanochromism and aggregation induced enhanced emission in phenothiazine substituted tetraphenylethylene, New J. Chem., 2019, 43, 16156-16163

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  • Y Rout, SM Mobin and R Misra*, Tetracyanobutadiene (TCBD) functionalized benzothiadiazole derivatives: effect of donor strength on the [2+2] cycloaddition–retroelectrocyclization reaction., New J. Chem., 2019, 43, 12299-12307.

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  • Y Rout, Y Jang, HB Gobeze, R Misra*, F D’Souza*, 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, J. Phys. Chem. C., 2019, 123, 23382-23389.

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  • B Carlotti*, M Poddar, F Elisei, A Spalletti and R Misra*, Energy-Transfer and Charge-Transfer Dynamics in Highly Fluorescent Naphthalimide–BODIPY Dyads: Effect of BODIPY Orientation, J. Phys. Chem. C., 2019, 123, 24362-24374.

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  • Y Patil, R Misra*, Rational molecular design towards NIR absorption: efficient diketopyrrolopyrrole derivatives for organic solar cells and photothermal therapy, J. Mater. Chem. C, 2019, 7, 13020-13031

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  • Y Patil, R Misra*, Metal Functionalized Diketopyrrolopyrroles: A Promising Class of Materials for Optoelectronic Applications, Chem. Rec., 2019, 19, 1-9.

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  • B Sekaran, Y Jang, R Misra*, F D’Souza, Push–Pull Porphyrins via β‐Pyrrole Functionalization: Evidence of Excited State Events Leading to High‐Potential Charge‐Separated States, Chem. Eur. J., 2019, 25, 12991-13001. *

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  • M Poddar, G Sivakumar, R Misra*, Donor–acceptor substituted 1,8-naphthalimides: design, synthesis, and structure–property relationship. J. Mater. Chem. C, 2019, 7, 14798-14815.

2018

  • A Ekbote, SH Han, T Jadhav, SM Mobin, JY Lee, R Misra*, Stimuli responsive AIE active positional isomers of phenanthroimidazole as non-doped emitters in OLEDs, J. Mater. Chem. C, 2018, 6, 2077-2087.

 

  • A Ekbote, SH Han, T Jadhav, SM Mobin, JY Lee, R Misra*, Stimuli responsive AIE active positional isomers of phenanthroimidazole as non-doped emitters in OLEDs, J. Mater. Chem. C, 2018, 6, 2077-2087.

 

  • Y Rout, R Misra*, R Singhal, S Biswas, GD Sharma, Phenothiazine-based small- molecules organic solar cells with power conversion efficiency over 7% and open circuit voltage of about 1.0 V using solvent vapor annealing, Phys. Chem. Chem. Phys., 2018, 20, 6321-6329.

 

  • Y Patil, C Popli, R Misra*, Near infrared absorbing tetracyanobutadiene bridged diketopyrrolopyrroles, New J. Chem., 2018, 42, 3892-3899.

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  • R Sharma, R Maragani, R Misra*, C3-Symmetric Star Shaped Donor-Acceptors truxenes: Synthesis, Photophysical, Electrochemical and computational studies, New J. Chem., 2018, 42, 882-890.

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  • MS Ansari, R Maragani, A Banik, R Misra*, M Qureshi, Enhanced photovoltaic performance using biomass derived nano 3D ZnO hierarchical superstructures and a D−A type CS-Symmetric triphenylamine linked bisthiazole, Electrochim. Acta, 2018, 259, 262-275.

 

  • Y Patil, R Misra*, Diketopyrrolopyrrole-Based and Tetracyano-Bridged Small Molecules for Bulk Heterojunction Organic Solar Cells, Chem. Asian J., 2018, 13, 220-229.

 

  • M Poddar, V Sharma, SM Mobin, R Misra*, 1,8‐Naphthalimide Substituted BODIPY Dyads: Synthesis, Structure, Properties and Live‐Cell Imaging, Chem. Asian J., 2018, 13, 2881-2890. *

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  • C Popli, Y Patil, R Misra*, Design and synthesis of N-phenyl carbazole substituted diketopyrrolopyrrole based monomers and dimers: A comparative study, Eur. J. Org. Chem., 2018, 6474-6481. [VIP Article]

 

  • S. Bijesh, R Misra*, Triphenylamine Functionalized Unsymmetrical Quinoxalines, Asian J. Org.Chem, 2018, 7, 1882-1892.

 

  • R Sharma, D Volyniuk, C Popli, O Bezvikonnyi, JV Grazulevicius, and R Misra*, Strategy Toward Tuning Emission of Star-Shaped Tetraphenylethene-Substituted Truxenes for Sky-Blue and Greenish-White Organic Light-Emitting Diodes, J. Phys. Chem. C, 2018, 122, 15614-15624.

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  • R Maragani, MB Thomas, R Misra*, and F D’Souza*‡, C3-Symmetric Positional Isomers of BODIPY Substituted Triazines: Synthesis and Excited State Properties, J. Phys. Chem. A, 2018, 122, 4829-4837.

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  • L Bucher, N Desbois, PD Harvey, CP Gros, R Misra*, and GD Sharma, Non-fullerene Polymer Solar Cells Reaching a 9.29% Efficiency Using a BODIPY-Thiophene Backboned Donor Material, ACS Appl. Energy Mater., 2018, 1, 3359-3368.

 

  • CR Seco, AV Ferran, R Misra*, GD Sharma, and E Palomares, Efficient Non-polymeric Heterojunctions in Ternary Organic Solar Cells, ACS Appl. Energy Mater., 2018, 1, 4203-4210.

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  • Y Patil, R Misra*, Small Molecule Based Non‐Fullerene Acceptors: A Comparative Study, Chem. Rec., 2018, 18, 1-16.

 

  • G Sivakumar, and R Misra*, Spiro-linked organic small molecules as hole-transport materials for perovskite solar cells, J. Mater. Chem. A, 2018, 6, 18750-18765.

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  • Y Patil, C Popli, R Misra*, Near infrared absorbing tetracyanobutadiene bridged diketopyrrolopyrroles, New J. Chem., 2018, 42, 3892-3899.

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  • R Sharma, R Maragani, R Misra*, C3-Symmetric Star Shaped Donor-Acceptors truxenes: Synthesis, Photophysical, Electrochemical and computational studies, New J. Chem., 2018, 42, 882-890.

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  • MS Ansari, R Maragani, A Banik, R Misra*, M Qureshi, Enhanced photovoltaic performance using biomass derived nano 3D ZnO hierarchical superstructures and a D−A type CS-Symmetric triphenylamine linked bisthiazole, Electrochim. Acta, 2018, 259, 262-275.

 

  • Y Patil, R Misra*, Diketopyrrolopyrrole-Based and Tetracyano-Bridged Small Molecules for Bulk Heterojunction Organic Solar Cells, Chem. Asian J., 2018, 13, 220-229.

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  • M Poddar, V Sharma, SM Mobin, R Misra*, 1,8‐Naphthalimide Substituted BODIPY Dyads: Synthesis, Structure, Properties and Live‐Cell Imaging, Chem. Asian J., 2018, 13, 2881-2890. *

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  • C Popli, Y Patil, R Misra*, Design and synthesis of N-phenyl carbazole substituted diketopyrrolopyrrole based monomers and dimers: A comparative study, Eur. J. Org. Chem., 2018, 6474-6481. [VIP Article]

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  • S. Bijesh, R Misra*, Triphenylamine Functionalized Unsymmetrical Quinoxalines, Asian J. Org.Chem, 2018, 7, 1882-1892.

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  • R Maragani, MB Thomas, R Misra*, and F D’Souza*‡, C3-Symmetric Positional Isomers of BODIPY Substituted Triazines: Synthesis and Excited  State Properties, J. Phys. Chem. A, 2018, 122, 4829-4837.

 

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  • Y Patil, R Misra*, Small Molecule Based Non‐Fullerene Acceptors: A Comparative Study, Chem. Rec., 2018, 18, 1-16.

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  • G Sivakumar, and R Misra*, Spiro-linked organic small molecules as hole-transport materials for perovskite solar cells, J. Mater. Chem. A, 2018, 6, 18750-18765.

2017

  • Anupama Ekbote, Thaksen Jadhav, Rajneesh Misra*, T-Shaped donor–acceptor–donor type tetraphenylethylene substituted quinoxaline derivatives: aggregation-induced emission and mechanochromism, New J. Chem.2017, 41, 9346–9353.

 

  • Madhurima Poddar, Rajneesh Misra*, NIR Absorbing Donor–Acceptor Based 1,1,4,4–Tetracyanobuta–1,3–Diene (TCBD) and Cyclohexa–2,5–Diene–1,4–Ylidene–Expanded TCBD SubstitutedFerrocenylPhenothiazines, Chem. Asian J. 2017,12,2908–2915. *

 

  • Yogajivan Rout, Prabhat Gautam and Rajneesh Misra*, Unsymmetrical and symmetrical push–pull phenothiazines, J. Org. Chem.2017, 82, 6840–6845.

 

  • Madhurima Poddar, Prabhat Gautam, Yogajivan Rout, Rajneesh Misra* Donor–acceptor phenothiazine functionalized BODIPYs, Dyes Pigm., 2017, 146,368–373.

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  • Yuvraj Patil, Rajneesh Misra*, Tetracyanobutadiene bridged ferrocene and triphenylamine functionalized pyrazabole dimers, J. Organomet. Chem., 2017, 840, 23–29.

 

  • Yuvraj Patil, JivanShinde, Rajneesh Misra*, Near-Infrared Absorbing Metal Functionalized Diketopyrrolopyrroles, J. Organomet. Chem., 2017, 852, 48–53.

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  • Ramesh Maragani, S. Bijesh, Rekha Sharma, Rajneesh Misra*,Cs-Symmetric Donor-Acceptor Bisthiazoles: Synthesis, Photophysical, Electrochemical and Computational Studies, AsianJ.Org. Chem., 2017, 6, 1408-1414.

 

  • Prabhat Gautam, Rajneesh Misra* and Michael Thomas, Francis D'Souza, Ultrafast charge separation in triphenylamine-BODIPY derived triads carrying centrally positioned, highly electron deficient, dicyanoquinodimethane or tetracyanobutadiene acceptors,Chem. Eur. J.2017,23, 9192–9200.

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  • Thaksen Jadhav, Jeong Min Choi, Jivan Shinde, Jun Yeob Lee and Rajneesh Misra*,Mechanochromism and electroluminescence in positional isomers of tetraphenylethylene substituted phenanthroimidazoles,J. Mater. Chem.C2017,5, 6014–6020.

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  • Ramesh Maragani, Mohammad Shaad Ansari, AvishekBanik, RajneeshMisra*, Mohammad Qureshi*, Cs-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 Omega2017,2, 5981–5991.

 

  • Yuvraj Patil, Rajneesh Misra* Manish Kumar Singh and Ganesh D Sharma, Ferrocene-diketopyrrolopyrrole based small molecule donor for bulk heterojunction solar cells,Phys. Chem. Chem. Phys.2017,19, 7262–7269.

 

  • Ramesh Maragani, Rekha Sharma, Rajneesh Misra*,Donor-Acceptor Triphenylvinyl and Tetraphenyl Conjugates: Synthesis, Aggregation and Computational Studies, ChemistrySelect2017,2, 10033–10037.

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  • Yuvraj Patil, Rajneesh Misra*, M. L.Keshtov, G. D. Sharma, Small molecule carbazole-​based diketopyrrolopyrroles with tetracyanobutadiene acceptor unit as a non-​fullerene acceptor for bulk heterojunction organic solar cells, J. Mater. Chem. A2017, 5, 3311–3319.

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  • Prabhat Gautam, Rahul Sharma, Rajneesh Misra*, M. L. Keshtov, S. A. Kuklin and Ganesh D. Sharma,  Donor–acceptor–acceptor (D–A–A) type 1,8-naphthalimides as non-fullerene small molecule acceptors for bulk heterojunction solar cells,Chem.Sci.2017,8, 2017–2024.​

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  • Ramesh Maragania, Rajneesh Misra*, M.S. Roy, Manish Kumar Singh and Ganesh D. Sharma, (D-p-A)2-p-D-A Type FerrocenylBisthiazole Linked Triphenylamine Based Molecular Systems for DSSC: Synthesis, Experimental and Theoretical Performance Studies, Phys. Chem. Chem. Phys.2017, 19, 8925–8933.

 

  • Yuvraj Patil, Thaksen Jadhav, Bhausaheb Dhokale, Holger Butenschoen, Rajneesh Misra* Donor Substituted Pyrazabole Monomers and Dimers: Design, Synthesis and Properties, ChemistrySelect, 2017,2, 415–420.

 

  • Rekha Sharma, Ramesh Maragani, RajneeshMisra*, Ferrocenylaza-dipyrromethene and aza-BODIPY: Synthesis and properties, J. Organomet.Chem. 2017, 825-826, 8–14.

 

  • Rajneesh Misra*, Thaksen Jadhav, Dustin Nevonen, Ellen M. Monzo, S. M. Mobin, Victor N. Nemykin, Synthesis, Structures, and Redox Properties of Tetracyano-Bridged Diferrocene Donor–Acceptor–Donor Systems, Organometallics2017,36, 4490–4498.

2016

  • Thaksen Jadhav, Bahusaheb Dhokale, Yuvraj Patil, S. M. Mobin, Rajneesh Misra*, Multi-Stimuli Responsive Donor–Acceptor Tetraphenylethylene Substituted Benzothiadiazoles,J. Phys. Chem. C2016, 120, 24030–24040.

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  • Bahusaheb Dhokale, Thaksen Jadhav, S. M. Mobin, Rajneesh Misra*, Tetracyanobutadiene functionalized ferrocenyl BODIPY dyes, Dalton Trans. 2016, 45, 1476–1483.

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  • T. S. Reddy, Ramesh Maragani, Rajneesh Misra*, Triarylborane substituted naphthalimide as a fluoride and cyanide ion sensor, Dalton Trans. 2016, 45, 2549–2553.

 

  • Ramesh Maragani, Prabhat Gautam, S. M. Mobin, RajneeshMisra*, C2-Symmetric ferrocenylbisthiazoles: synthesis, photophysical, electrochemical and DFT studies, Dalton Trans. 2016, 45, 4802–4809.​

 

  • Bahusaheb Dhokale, Thaksen Jadhav, Yuvraj Patil, RajneeshMisra*, Symmetrical and unsymmetrical ferrocenylperylenediimides: Design, synthesis and properties. Dyes Pigm. 2016, 134, 164–170.

 

  • Yuvraj Patil, Thaksen Jadhav, Bahusaheb Dhokale, Rajneesh Misra*, Design and Synthesis of Low HOMO–LUMO Gap N-Phenylcarbazole-Substituted Diketopyrrolopyrroles, Asian J. Org. Chem. 2016, 5, 1008–1014.

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  • T. S. Reddy, Ramesh Maragani, Bahusaheb Dhokale, S. M. Mobin, Rajneesh Misra*, Heteroatom-connected ferrocenyl substituted naphthalimides, RSC Adv. 2016, 6, 7746–7754.

 

  • Yuvraj Patil, Thaksen Jadhav, Bahusaheb Dhokale, Rajneesh Misra*, Tuning of the HOMO–LUMO Gap of Symmetrical and Unsymmetrical Ferrocenyl-Substituted Diketopyrrolopyrroles, Eur. J. Org. Chem. 2016, 733–738.

 

  • Ramesh Maragani, T.S. Reddy, Rajneesh Misra*, CS-symmetric triarylborane substituted bisthiazole for selective detection of F− and CN− ions, Tetrahedron Lett. 2016, 57, 3853–3857.

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  • Rekha Sharma, Ramesh Maragani, RajneeshMisra*, Ferrocenylaza-dipyrromethene and aza-BODIPY: Synthesis and properties, J. Organomet. Chem. 2016, 825, 8–14.​

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  • Yuvraj Patil, Rajneesh Misra*, M. L. Keshtov, G. D. Sharma, 1,1,4,4-Tetracyanobuta-1,3-diene Substituted Diketopyrrolopyrroles: An Acceptor for Solution Processable Organic Bulk Heterojunction Solar Cells, J. Phys. Chem. C2016,120, 6324–6335.

 

  • Thaksen Jadhav, J. M. Choi, Bahusaheb Dhokale, S. M. Mobin, J. Y. Lee, Rajneesh Misra*, Effect of End Groups on Mechanochromism and Electroluminescence in Tetraphenylethylene Substituted Phenanthroimidazoles, J. Phys. Chem. C2016, 120,18487–18495.

 

  • Prabhat Gautam, Rajneesh Misra*, G. D. Sharma, Dicyanoquinodimethane-substituted benzothiadiazole for efficient small-molecule solar cells, Phys. Chem. Chem. Phys. 2016, 18, 7235–7241.

 

  • Prabhat Gautam, Rajneesh Misra*, S. Biswas, G. D. Sharma, A D–π–A1–π–A2 push–pull small molecule donor for solution processed bulk heterojunction organic solar cells, Phys. Chem. Chem. Phys. 2016, 18, 13918–13926.

 

  • Yuvraj Patil, Rajneesh Misra*, F. C. Chen, G. D. Sharma, Small molecule based N-phenyl carbazole substituted diketopyrrolopyrroles as donors for solution-processed bulk heterojunction organic solar cells,Phys. Chem. Chem. Phys. 2016, 18, 22999–23005.

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  • Yuvraj Patil, Rajneesh Misra*, A. Sharma, G. D. Sharma, D–A–D–π–D–A–D type diketopyrrolopyrrole based small molecule electron donors for bulk heterojunction organic solar cell, Phys. Chem. Chem. Phys. 2016, 18, 16950–16957.

 

  • Rajneesh Misra*, Ramesh Maragani, C. P. Singh, R. Chari, Photonic properties of star shaped ferrocenyl substituted triazines, Dyes Pigm.  2016, 126, 110–117.

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  • Rajneesh Misra*, Ramesh Maragani, D. Arora, A. Sharma, G. D. Sharma, Positional isomers of pyridine linked triphenylamine-based donor-acceptor organic dyes for efficient dye-sensitized solar cells, Dyes Pigm.  2016, 126, 38–45.

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  • Thaksen Jadhav, J. M. Choi, J. Y. Lee, Bahusaheb Dhokale, Rajneesh Misra*, Non-doped blue organic light emitting devices based on tetraphenylethylene-π-imidazole derivatives, Organic Electronics2016, 37, 448–452.

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  • Yuvraj Patil, Rajneesh Misra*, F. C. Chen, M. L. Keshtov, G. D. Sharma, Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells, RSC Adv. 2016, 6, 99685–99694.

2015

  • Rajneesh Misra*, Thaksen Jadhav, Bahusaheb Dhokale and S. M. Mobin, Colorimetric and Fluorimetric Detection of Fluoride and Cyanide Ions Using Tri and Tetra Coordinated Boron Containing Chromophores, Dalton Trans. 2015, 44, 16052–16060.

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  • Rajneesh Misra*, Ramesh Maragani,BiswarupPathak,Prabhat Gautam and S. M. Mobin,Star shaped Ferrocenyl Substituted Triphenylamines, RSC Adv.2015,5, 71046–71051.

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  • Rajneesh Misra*, Prabhat Gautam, Ramesh Maragani, Ferrocenylthiazoles: Synthesis and properties, Tetrahedron Lett. 2015,56, 1664–1666.

 

  • Rajneesh Misra*, Prabhat Gautam,Meso-tetrakis(ferrocenylethynylphenyl) porphyrins: Synthesis and properties, J. Organomet. Chem. 2015,776,83–88.

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  • Prabhat Gautam,Rajneesh Misra*, Shahbaz A. Siddiqui and Ganesh D. Sharma, Unsymmetrical Donor–Acceptor–Acceptor−π–Donor Type Benzothiadiazole-Based Small Molecule for a Solution Processed Bulk Heterojunction Organic Solar Cell, ACS Appl. Mater. Interfaces,2015,7,10283–10292.

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  • Thaksen Jadhav, Rajneesh Misra*, S. Biswas,Ganesh D. Sharma,Bulk heterojunction organic solar cells based on carbazole-BODIPY conjugate small molecules as donors with high open circuit voltage Bulk heterojunction organic solar cells based on carbazole-BODIPY conjugate small molecules as donors with high open circuit voltage,  Phys .Chem. Chem. Phys. 2015,17, 26580–26588.

 

  • Prabhat Gautam, RajneeshMisra*, Shahbaz A. Siddiqui, Ganesh D. Sharma,  Donor–acceptor–π–acceptor based charge transfer chromophore as electron donors for solution processed small molecule organic bulk heterojunction solar cells, Org. Electron.,2015,19,76–82.

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  • Rekha Sharma, Prabhat Gautam, Rajneesh Misra* and Sanjeev K. Shukla, β-Substituted triarylborane appended porphyrins: photophysical properties and anion sensing, RSC Adv.2015,5, 27069–27074.

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  • Ganesh D. Sharma,* K.R. Patel, M.S. Roy, Rajneesh Misra, Characterization of two new (A–π) 2–D–A type dyes with different central D unit and their application for dye sensitized solar cells, Org. Electron. 2015,15,1780–1790.

 

  • Thaksen Jadhav, Bahusaheb Dhokale, Shaikh M. Mobin, RajneeshMisra*, Mechanochromism and aggregation induced emission in benzothiazole substituted tetraphenylethylenes: a structure function correlation, RSC Adv. 2015,5,29878–29884.

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  • Thaksen Jadhav, Bahusaheb Dhokale, RajneeshMisra*, Effect of the cyano group on solid state photophysicalbehavior of tetraphenylethene substituted benzothiadiazoles, J.  Mater. Chem. C,2015,27,9063–9068.

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  • Prabhat Gautam, Ramesh MaraganiRajneesh Misra* Aryl-substituted symmetrical and unsymmetrical benzothiadiazoles, RSC Adv.2015,5,18288–18294 . 

 

  • BhausahebDhokale, Thaksen Jadhav, Shaikh M. Mobin,RajneeshMisra*, Mesoenyne substituted

       BODIPYs: synthesis, structure and properties, DaltonTrans. 2015, 44,15803–15812.

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  • Thaksen Jadhav, BhausahebDhokale, Shaikh M. Mobin, Rajneesh Misra*, Mechanochromism and aggregation induced emission in benzothiazole substituted tetraphenylethylenes: a structure function correlation, RSC Adv.2015,5,29878–29884.

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  • Thaksen Jadhav, BahuahebDhokale, Shaikh M. Mobin, Rajneesh Misra*, Aggregation induced emission and mechanochromism inpyrenoimidazoles, J. Mater. Chem. C 2015,3,9981–9988.

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  • Bahusaheb Dhokale, Thaksen Jadhav, Shaikh M. Mobin, Rajneesh Misra*, Synergistic effect of donors on tetracyanobutadine (TCBD) substituted ferrocenyl pyrenes, RSC Adv.2015,5, 57692–57699.

 

  • Bahusaheb Dhokale,Thaksen Jadhav, Shaikh M. Mobin, Rajneesh Misra*, MesoAlkynylatedTetraphenylethylene (TPE) and 2, 3, 3-Triphenylacrylonitrile (TPAN) Substituted BODIPYs, J. Org. Chem. 2015, 80, 8018–8025.

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  • Thaksen Jadhav, BhausahebDhokale, Yuvraj Patil Rajneesh Misra*, Aggregation induced emission and mechanochromism in tetraphenylethene substituted pyrazabole, RSC Adv., 2015, 5, 68187–68191.

2014

  • Rajneesh Misra*, Thaksen Jadhav, Shaikh M. Mobin, Ferrocenylpyrazaboles: design, synthesis, structure, and properties, Dalton Trans. 2014, 43, 2013–2022.

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  • Rajneesh Misra*, BhausahebDhokale, Thaksen Jadhav, Shaikh M. Mobin, Quenching of fluorescence as an indicator of donor-strength in mesoarylethynyl BODIPYs, Dalton Trans. 2014, 43, 4854–4861.​

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  • Rajneesh Misra*, Rekha Sharma and Shaikh M. Mobin, Star shaped ferrocenyltruxenes: synthesis, structure and properties, Dalton Trans. 2014, 43, 6891–6896.

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  • Rajneesh Misra*, BhausahebDhokale, Thaksen Jadhav, Shaikh M. Mobin, Heteroatom, connected ferrocenyl BODIPYs: synthesis, structure and properties, Organometallics 2014, 33, 1867−1877.

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  • Rajneesh Misra*, Prabhat Gautam, Tuning of the HOMO-LUMO gap of donor substituted symmetrical and unsymmetrical benzothiadiazoles, Org. Biomol. Chem.2014, 12, 5448–5457.

 

  • Rajneesh Misra*, Thaksen Jadhav, BhausahebDhokale, and Shaikh M. Mobin, Reversible mechanochoromism and enhanced AIE in triphenylethene substituted phenanthroimidazoles,  ChemCommun.2014, 50, 9076–9078.

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  • Rajneesh Misra*, Thaksen Jadhav, BhausahebDhokale, Prabhat Gautam, Rekha Sharma, Ramesh Maragani and Shaikh M. Mobin, Carbazole-BODIPY conjugates: design, synthesis, structure and properties, Dalton Trans. 2014, 43, 13076–13086.

 

  • Rajneesh Misra*, Ramesh Maragani, Prabhat Gautam, Shaikh M. Mobin, Tetracyanoethylene substituted triphenylamine analogues, Tetrahedron Lett. 2014, 55, 7102–7105.

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  • Rajneesh Misra*, BhausahebDhokale, Thaksen Jadhav, and Shaikh M. Mobin, Meso- aryloxy and meso-arylaza linked BODIPY dimers: synthesis, New J. Chem.2014,38, 3579–3585.

 

  • Rajneesh Misra*, Ramesh Maragani, K. R. Patel and Ganesh D. Sharma, Synthesis, optical and electrochemical properties of new ferrocenyl substituted triphenylamine based donor–acceptor dyes for dye sensitized solar cells, RSC Adv.2014, 4, 34904–34911.

 

  • Ramesh Maragani,Rajneesh Misra*, Ferrocenyl Substituted triphenylamine based donor–acceptor molecular systems; synthesis, photophysical, electrochemical, and theoretical studies, Tetrahedron 2014, 70, 3390–3399.

 

  • BhausahebDhokale, Thaksen Jadhav, Shaikh M. Mobin, Rajneesh Misra*,Meso enamine substituted BODIPYs,ChemCommun.2014, 50, 9119–9121.

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  • Prabhat Gautam, Ramesh Maragani, Shaikh M. Mobin,Rajneesh Misra*,Reversiblemechanochoromism in dipyridyl amine substituted, unsymmetrical benzothiadiazoles,RSC Adv.2014,4, 52526–52529.

 

  • C.P. Singh, Rekha Sharma, V. Shukla, P. Khundrakpam, Rajneesh Misra*, K.S. Bindra, Rama Chari, Optical limiting and nonlinear studies of ferrocenyl substituted calixarenes,Chem.Phy. Lett.2014, 616, 189–195.

 

  • Satya Narayan Sahu, ManeeshKumar Gupta, Thaksen Jadhav, Pratik Yadav, Surjeet Singh, Rajneesh Misra* and RamendraPratap, Substitutent dependent tunable fluorescence in thieno [3,2-c] pyrans, RSC Adv.2014,4, 56779–56783.

2013

  • Rajneesh Misra*, Prabhat Gautam, S. M. Mobin, Aryl- substituted unsymmetrical benzothiadiazoles: Synthesis, Structure, and properties, J. Org. Chem. 2013,78, 12440–12452.

 

  • Rajneesh Misra*, Thaksen Jadhav, Shaikh M. Mobin, Aryl Pyrazaboles: A new class of tunable and highlyfluorescent materials, Dalton Trans. 2013,42, 16614–16620.

 

  • Rajneesh Misra*, Prabhat Gautam, Thaksen Jadhav, S. M. Mobin, Donor acceptor ferrocenyl substituted benzo- thiadiazoles: Synthesis, Structure, J. Org. Chem. 2013, 78, 4940–4948.

 

  • Rajneesh Misra*, BhausahebDhokale, Thaksen Jadhav, S. M. Mobin, Donor acceptor ferrocenyl BODIPYs with marvellous supramolecular intereactions, Dalton Trans. 2013,42, 13658–13666.

 

  • Rajneesh Misra*, Ramesh  Maragani, Thaksen Jadhav, S. M. Mobin, Ferrocenyl end capped molecular rods: Synthesis, Structure, and properties,New J. Chem.2013,38, 1446–1457.

 

  • Rajneesh Misra*, Prabhat Gautam, Rekha Sharma, S. M. Mobin, Donor acceptor ferrocenylbenzothiadiazoles: Synthesis, Structure, and properties, Tetrahedron Lett. 2013,54, 381–383.

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  • Ramesh Maragani, Rajneesh Misra* Donor-acceptor ferrocenyltriazenes: synthesis and properties, Tetrahedron Lett. 2013,54, 5399–5402.

 

  • Thaksen Jadhav, Ramesh Maragani, Rajneesh Misra*, V. Sreeramulu, D. NarayanaRao, Shaikh M. Mobin, Design and synthesis of donor-acceptor pyrazoble derivatives for multiphoton absorption, Dalton Trans. 2013,42, 4340–4342.

 

  • Bhausaheb Dhokale, Prabhat Gautam, S. M. Mobin, Rajneesh Misra* Donor acceptor ferrocenyl BODIPYs with marvelous supramolecular intereactions,Dalton Trans.2013,42, 1512–1518.

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  • Rekha Sharma, Prabhat Gautam, S. M. Mobin,RajneeshMisra*, beta-substituted ferrocenyl porphyrins: synthesis, structure and properties, Dalton Trans. 2013,42, 5539–5545.

 

  • ​Ramesh Maragani, Thaksen Jadhav, Shaikh M. Mobin,RajneeshMisra*, C3 symmetric ferrocenyltriazines: syntesis, structure, and properties, RSC Adv.2013, 3, 2888–2892.

 

  • Rekha Sharma, Ramesh Maragani, S. M. Mobin,RajneeshMisra*, Ferrocenyl substituted calixarenes: synthesis structure and properties, RSCAdv.2013,3, 5785–5788.

2012

  • Prabhat Gautam, BhausahebDhokale, S. M. Mobin, RajneeshMisra*, Ferrocenyl BODIPYs: synthesis, structure and properties, RSC Adv.2012,2, 12105–12107. 

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  • Bhausaheb Dhokale, Prabhat Gautam,Rajneesh Misra*, Donor-Acceptor Perylenediimide-Ferrocene conjugates: synthesis, photophysical, and electrochemical properties, Tetrahedron Lett. 2012,53, 2352–2354​

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  • Ramesh Maragani, Thaksen Jadhav, Shaikh M. Mobin, Rajneesh Misra*, Synthesis, structure, photophysical, and electrochemical properties of donor acceptor ferrocenyl derivatives, Tetrahedron Lett. 2012,68, 7302–7308.

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  • Prabhat Gautam, Bahusaheb Dhokale, V. Shukla, C. P. Singh, K. S. Bindra, Rajneesh Misra*, Spectacular optical limiting performance of meso-tetraferrocenylporphyrin, and its metal derivative, J. Photochem. &Photobio. A: Chem. 2012, 239, 24 – 27.

FromPhD and Postdoc

  • Xiaowei Zhan, Zhan'ao Tan, Erjun Zhou, Yongfang Li, Rajneesh Misra , Adrian Grant, Benoit Domercq, Xiao-Hong Zhang, Zesheng An, Xuan Zhang, Stephen Barlow, Bernard Kippelen, Seth R. Marder*,  Copolymers of perylenediimide with dithienothiophene and dithienopyrrole as electron-transport materials for all-polymer solar cells and field-effect transistors, J. Mater. Chem.2009,19, 5794–5803.

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  • Rajneesh Misra, T. K. Chandrashekar*, Structural Diversity in Expanded Porphyrins, Acc. Chem. Res.2008,41, 265–279.

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  • Min-Chul Yoon, Rajneesh Misra, ZinSeok Yoon, Mi Kyung Ko, Jung Ho Kwon, Su Bum Noh,Tavarekere K. Chandrashekar* and Dongho Kim,  Photophysical study of core-modified expanded porphyrins: nature of aromaticity and enhancement of ring-planarity,  J. Phys. Chem. B2008, 112, 6900–6905.

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  • RajneeshMisra, R. Kumar, T. K.Chandrashekar*, B. S. Joshi, 26 Aromatic Core-Modified Hexaphyrins: Syntheses, Characterizat-ion, and structural diversities, J. Org. Chem.2007,72, 1153–1160.

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  • R. Kumar, Rajneesh Misra, T. K.Chandrashekar*, E. Suresh, Near IR absorbing planar aromatic[34]octaphyrins(1.1.0.1.1.0.0.0) containing a quaterthiophene subunit,  Chem. Commun. 2007, 43–45.

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  • R. Kumar, RajneeshMisra, T. K. Chandrashekar, E. Suresh, A. Nag, D Goswami,  One Pot Synthesis of Core-Modified RubyrinOctaphyrin and Dodecaphyrin: Synthesis, Characterization and Nonlinear Optical Properties, Eur. J. Org. Chem. 2007,27, 4552–4562.

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Department of Chemistry,

School of Basic Sciences,

Indian Institute of Technology Indore, Simrol, Indore 453552, India

PhD Positions Available

Post Doctoral Positions Available 

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