{"id":166,"date":"2025-07-14T19:52:07","date_gmt":"2025-07-14T19:52:07","guid":{"rendered":"https:\/\/rockstartesting.in\/rajamalli\/?page_id=166"},"modified":"2025-10-27T06:15:29","modified_gmt":"2025-10-27T06:15:29","slug":"publications","status":"publish","type":"page","link":"https:\/\/rockstartesting.in\/rajamalli\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\t\t
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Publications<\/h1>\t\t\t\t<\/div>\n\t\t\t\t
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Our publication Showcases latest research breakthroughs in materials design and device innovation.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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\n \n \n 2011<\/span>\n\n \n
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  1. Low Molecular Weight Fluorescent Organogel for Fluoride Ion Detection,\u00a0P. Rajamalli<\/strong>\u00a0and E. Prasad,\u00a0Org. Lett.,<\/em>\u00a02011<\/strong>,\u00a013<\/em>, 3714.\u00a010.1021\/ol201325j<\/strong><\/a><\/li>
  2. Luminescent Micro and Nanogel Formation from\u00a0AB3\u00a0type Poly(Aryl Ether) Dendron Derivatives\u00a0without\u00a0Conventional Multi-Interactive Gelation\u00a0Motifs,\u00a0P. Rajamalli<\/strong>\u00a0and\u00a0E. Prasad,\u00a0New J. Chem.<\/em>,\u00a02011<\/strong>,\u00a035<\/em>, 1541.\u00a010.1039\/c1nj20136k<\/strong><\/a><\/li><\/ol> <\/div>\n\n <\/div>\n\n <\/div>\n\n \n
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    \n \n \n 2012<\/span>\n\n \n
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    1. Non-Amphiphilic\u00a0Pyrene Cored Poly(Aryl Ether) Dendron Based Gels: Tunable Morphology, Unusual Solvent Effects on the Emission and Fluoride Ion Detection by the Self-Assembled Superstructures,\u00a0P. Rajamalli<\/strong>\u00a0and\u00a0E. Prasad,\u00a0Soft Matter<\/em>,\u00a02012<\/strong>,\u00a08<\/em>, 8896.\u00a010.1039\/c2sm26151k<\/strong><\/a><\/li><\/ol> <\/div>\n\n <\/div>\n\n <\/div>\n\n \n
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      \n \n \n 2013<\/span>\n\n \n
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      1. Glucose-cored Poly(Aryl Ether) Dendron based Low Molecular Weight Gels: PH Controlled Morphology and Hybrid Hydrogel Formation.,\u00a0P. Rajamalli<\/strong>, P. S. Sheet and E. Prasad,\u00a0Chem. Commun.<\/em>,\u00a02013<\/strong>,\u00a049<\/em>, 6758.\u00a010.1039\/c3cc43391a<\/strong><\/a><\/li>
      2. Supramolecular Design for Two-Component Hydrogels with Intrinsic Emission in the Visible Region,\u00a0P. Rajamalli<\/strong>,\u00a0S. Atta, S. Maity\u00a0and\u00a0E. Prasad,Chem. Commun.<\/em>,2013<\/strong>,\u00a049<\/em>, 1744.\u00a010.1039\/c3cc38419e<\/strong><\/a><\/li>
      3. Tunable Morphology and Mesophase Formation by Naphthalene-Containing Poly(Aryl Ether) Dendron-Based Low-Molecular-Weight Fluorescent Gels,\u00a0P. Rajamalli<\/strong>\u00a0and E. Prasad,\u00a0Langmuir<\/em>,\u00a02013<\/strong>,\u00a029<\/em>, 1609.\u00a010.1021\/la304230m<\/strong><\/a><\/li><\/ol> <\/div>\n\n <\/div>\n\n <\/div>\n\n \n
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        \n \n \n 2014<\/span>\n\n \n
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        1. Palladium-Catalyzed Dehydrogenative \u03b2\u2011arylation of Simple Saturated Carbonyls by Aryl Halides, P. Gandeepan,\u00a0P. Rajamalli<\/strong>\u00a0and C.-H. Cheng,\u00a0ACS Catal.,\u00a0<\/em>2014<\/strong>,\u00a04<\/em>, 4485.\u00a010.1021\/cs501326p<\/strong><\/a><\/li>
        2. Metal Induced Gelation from Pyridine Cored Poly(Aryl Ether) Dendrons with In Situ Synthesis and Stabilization of Hybrid Hydrogel Composites,\u00a0P. Rajamalli<\/strong>, P. Malakar, S. Atta, and E. Prasad,\u00a0Chem. Commun.<\/em>, 2014,\u00a050<\/em>, 11023.\u00a010.1039\/C4cc04231j<\/strong><\/a>\u00a0<\/li>
        3. Highly Efficient Orange and Deep-Red Organic Light Emitting Diodes with Long Operational Lifetime using Carbazole-Quinoline based Bipolar Host MaterialsC.-H. Chen, L.-C. Hsu,\u00a0P. Rajamalli<\/strong>, Y.-W. Chang, F.-I. Wu, C.-Y. Liao, M.-J. Chiu, P.-Y. Chou, M.-J. Huang, L.-K. Chu and C.-H. Cheng,\u00a0J. Mater. Chem. C<\/em>,\u00a02014<\/strong>,\u00a02<\/em>, 6183.\u00a010.1039\/c4tc00523f<\/strong><\/a><\/li>
        4. Synthesis of Substituted Quinolines by Iron(iii)-Catalyzed Three-Component Coupling Reaction of Aldehydes, Amines and Styrenes, P. Gandeepan,\u00a0P. Rajamalli<\/strong>\u00a0and C.-H. Cheng,\u00a0Asian J. Org. Chem.<\/em>,\u00a02014<\/strong>,\u00a03<\/em>, 303.\u00a010.1002\/ajoc.201300262<\/strong><\/a><\/li><\/ol> <\/div>\n\n <\/div>\n\n <\/div>\n\n \n
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          \n \n \n 2015<\/span>\n\n \n
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          1. m<\/em>-Indolocarbazole Derivative as A Universal Host Material for RGB and White Phosphorescent OLEDs, C.-C. Lai, M.-J. Huang, H.-H. Chou, C.-Y. Liao,\u00a0P. Rajamalli<\/strong>\u00a0and C.-H. Cheng,\u00a0Adv. Funct. Mater.<\/em>,\u00a02015<\/strong>,\u00a025<\/em>, 5548.\u00a010.1002\/adfm.201502079<\/strong><\/a><\/li>
          2. A Universal Electron-Transporting\/Exciton-Blocking Material for Blue, Green, and Red Phosphorescent Organic Light-Emitting Diodes (OLEDs), C.-H. Shih,\u00a0P. Rajamalli<\/strong>, C.-A. Wu, W.-T. Hsieh and C.-H. Cheng,\u00a0ACS Appl. Mater. Interfaces,\u00a0<\/em>2015<\/strong>,\u00a07<\/em>, 10466.\u00a010.1021\/acsami.5b01872<\/strong><\/a><\/li>
          3. Rhodium(III)-catalyzed [4+1] Annulation of Aromatic and Vinylic Carboxylic Acids with Allenes: An Efficient Method Towards Vinyl-Substituted Phthalides and 2-furanones, P. Gandeepan,\u00a0P. Rajamalli<\/strong>\u00a0and C.-H. Cheng,\u00a0Chem. -Eur. J.<\/em>,\u00a02015<\/strong>,\u00a021<\/em>, 9198.\u00a010.1002\/chem.201501106<\/strong><\/a><\/li>
          4. Bromo Induced Reversible Distinct Switching of Emission of Anthracence-Based Donor-Acceptor Compound by Vapo, Piezo and Thermal Stimuli,\u00a0P. Rajamalli<\/strong>, P. Gandeepan, M.-J. Huang and C.-H. Cheng,\u00a0J. Mater. Chem. C<\/em>,\u00a02015<\/strong>,\u00a03<\/em>, 3329.\u00a010.1039\/c5tc00109a<\/strong><\/a><\/li>
          5. A High Triplet Energy, High Thermal Stability Oxadiazole Derivative as The Electron Transporter for Highly Efficient Red, Green and Blue Phosphorescent OLEDs, C.-H. Shih,\u00a0P. Rajamalli<\/strong>, C.-A. Wu, M.-J. Chiu, L.-K. Chu and C.-H. Cheng,\u00a0J. Mater. Chem. C<\/em>,\u00a02015<\/strong>,\u00a03<\/em>, 1491.\u00a010.1039\/c4tc02348j<\/strong><\/a><\/li><\/ol> <\/div>\n\n <\/div>\n\n <\/div>\n\n \n
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            \n \n \n 2016<\/span>\n\n \n
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            1. An Effective Strategy for Reducing the Singlet-Triplet Energy Gaps of TADF Materials for Improving the Blue OLED Efficiency,\u00a0P. Rajamalli<\/strong>, N. Senthilkumar, P. Gandeepan, and C.-H. Cheng,\u00a0ACS Appl. Mater. Interfaces<\/em>,\u00a02016<\/strong>,\u00a08<\/em>, 27026.\u00a010.1021\/acsami.6b10678<\/strong><\/a><\/li>
            2. A New Molecular Design based on Thermally Activated Delayed Fluorescence for Highly Efficient Organic Light Emitting Diodes,\u00a0P. Rajamalli<\/strong>, N. Senthilkumar, P. Gandeepan, P.-Y. Huang, M.-J. Huang, C.-Z. Ren-Wu, C.-Y. Yang, M.-J. Chiu, L.-K. Chu, H.-W. Lin and C.-H. Cheng,\u00a0J. Am. Chem. Soc.<\/em>\u00a02016<\/strong>,\u00a0138<\/em>, 628.\u00a010.1021\/jacs.5b10950<\/strong><\/a><\/li>
            3. A Thermally Activated Delayed Blue Fluorescent Emitter with Reversible Externally Tunable Emission,\u00a0P. Rajamalli<\/strong>, N. Senthilkumar, P. Gandeepan, C.-Z. Ren-Wu, H.-W. Lin and C.-H. Cheng,\u00a0J. Mater. Chem. C,\u00a0<\/em>2016<\/strong>,\u00a04<\/em>, 900.\u00a010.1039\/c5tc03943f<\/strong><\/a><\/li>
            4. Diastereoselective [3+2] Annulation of Aromatic\/Vinylic Amides with Bicyclic Alkenes via A Cobalt-Catalyzed C-H Activation and Intramolecular Nucleophilic Addition, P. Gandeepan,\u00a0P. Rajamalli<\/strong>\u00a0and C.-H. Cheng,\u00a0Angew. Chem. Int. Ed.<\/em>,\u00a02016<\/strong>,\u00a055<\/em>, 4308.\u00a010.1002\/anie.201512018<\/strong><\/a><\/li>
            5. Palladium-Catalyzed C-H Activation and Cyclization of Anilides with 2-Iodoacetates and 2-Iodobenzoates: An Efficient Method Toward Oxindoles and Phenanthridones, P. Gandeepan,\u00a0P. Rajamalli<\/strong>\u00a0and C.-H. Cheng,\u00a0Synthesis<\/em>,\u00a02016<\/strong>,\u00a048<\/em>, 1872.\u00a010.1055\/s-0035-1561856<\/strong><\/a><\/li>
            6. Copper-Promoted Multiple Aza-[4 + 2] Cycloaddition Reactions between Benzylic Azides and Alkenes, W.-C. Chen, P. Gandeepan, C.-H. Tsai, C.-Z. Luo,\u00a0P. Rajamalli<\/strong>\u00a0and C.-H. Cheng,\u00a0RSC Advances<\/em>,\u00a02016<\/strong>,\u00a06<\/em>, 63390.\u00a010.1039\/c6ra11840b<\/strong><\/a><\/li><\/ol> <\/div>\n\n <\/div>\n\n <\/div>\n\n \n
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              \n \n \n 2017<\/span>\n\n \n
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              1. New Molecular Design Concurrently Providing Superior Pure Blue, Thermally Activated Delayed Fluorescence and Optical Out-Coupling Efficiencies,\u00a0P. Rajamalli<\/strong>, N. Senthilkumar, P.-Y. Huang, C.-C. Ren-Wu, H.-W. Lin, and C.-H. Cheng,\u00a0J. Am. Chem. Soc.<\/em>,\u00a02017<\/strong>,\u00a0139<\/em>, 10948.\u00a010.1021\/jacs.7b03848<\/strong><\/a><\/li>
              2. Thermally Activated Delayed Fluorescence Emitters with A\u00a0m<\/em>,m<\/em>-Di-Tert<\/em>-Butyl-Carbazolyl Benzoylpyridine Core Achieving Extremely high Blue Electroluminescence Efficiencies,\u00a0P. Rajamalli<\/strong>, V. Thangaraji, N. Senthilkumar, C.-C. Ren-Wu, H.-W. Lin, and C.-H. Cheng,\u00a0J. Mater. Chem. C<\/em>,\u00a02017<\/strong>,\u00a05<\/em>, 2919.\u00a010.1039\/c7tc00457e<\/strong><\/a><\/li><\/ol> <\/div>\n\n <\/div>\n\n <\/div>\n\n \n
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                \n \n \n 2018<\/span>\n\n \n
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                1. Marigold Flower-Like Assemblies of Phosphorescent Iridium-Silver Coordination Polymers, D. Rota Martir,\u00a0P. Rajamalli<\/strong>, D. B. Cordes, A. M. Z. Slawin and E. Zysman-Colman,\u00a0Macromol. Rapid Commun.,\u00a0<\/em>2018<\/strong>, 1800501.\u00a010.1002\/marc.201800501<\/strong><\/a><\/li>
                2. Molecular Design Strategy for a Two-Component Gel Based an a Thermally Activated Delayed Fluorescence Emitter,\u00a0P. Rajamalli<\/strong>, D. Rota\u2005Martir, E. Zysman-Colman,\u00a0ACS Appl. Energy Mater.<\/em>,\u00a02018<\/strong>,\u00a01<\/em>,\u00a0649.\u00a010.1021\/acsaem.7b00161<\/strong><\/a><\/li>
                3. Pyridine-Functionalized Carbazole Donor and Benzophenone Acceptor Design for Thermally Activated Delayed Fluorescence Emitters in Blue Organic Light Emitting Diodes,\u00a0P. Rajamalli<\/strong>, D. Rota\u2005Martir, E. Zysman-Colman,J. Photon. Energy<\/em>,\u00a02018<\/strong>,\u00a08<\/em>, 032106.\u00a010.1117\/1.jpe.8.032106<\/strong><\/a><\/li><\/ol> <\/div>\n\n <\/div>\n\n <\/div>\n\n <\/div>\n <\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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                  \n \n \n 2019<\/span>\n\n \n
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                  1. Improving Processability and Efficiency of Resonant TADF emitters: A Design Strategy, D. Hall, S. M. Suresh, P. L. dos Santos, E. Duda, S. Bagnich, A. Pershin,\u00a0P. Rajamalli<\/strong>, D. B. Cordes, A. M. Z. Slawin, D. Beljonne, A. K\u0161hler, I. D. W. Samuel, Y. Olivier and E. Zysman-Colman,\u00a0Adv. Optical Mater.<\/em>,\u00a02019<\/strong>, 1901627.\u00a010.1002\/adom.201901627<\/a><\/strong>