| Year |
Citation |
Score |
| 2023 |
Yadav I, Sankar M. Panchromatic and Perturbed Absorption Spectral Features and Multiredox Properties of Dicyanovinyl- and Dicyanobutadienyl-Appended Cobalt Corroles. Inorganic Chemistry. 62: 19956-19970. PMID 38010211 DOI: 10.1021/acs.inorgchem.3c02666 |
0.683 |
|
| 2023 |
Shanu M, Acharyya JN, Sankar M, Vijaya Prakash G. Enhanced Femtosecond Nonlinearities and Multiphoton Absorptions in Discrete Bands of Porphyrins. Inorganic Chemistry. 62: 12895-12904. PMID 37523680 DOI: 10.1021/acs.inorgchem.3c01585 |
0.354 |
|
| 2023 |
Tasleem M, Yadav M, Ganesan V, Sankar M. Co(II) Porphyrin-MWCNT Nanoconjugate as an Efficient and Durable Electrocatalyst for Oxygen Reduction Reaction. Langmuir : the Acs Journal of Surfaces and Colloids. 39: 8075-8082. PMID 37264648 DOI: 10.1021/acs.langmuir.3c00380 |
0.759 |
|
| 2023 |
Yadav I, Osterloh WR, Kadish KM, Sankar M. Synthesis, Spectral, Redox, and Sensing Studies of β-Dicyanovinyl-Appended Corroles and Their Metal Complexes. Inorganic Chemistry. PMID 37146287 DOI: 10.1021/acs.inorgchem.3c00341 |
0.685 |
|
| 2023 |
Yadav I, Sharma JK, Sankar M, D'Souza F. Symmetrically Functionalized Copper and Silver Corrole-Bis-Tetracyanobutadiene Push-Pull Conjugates: Efficient Population of Triplet States via Charge Transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301341. PMID 37133307 DOI: 10.1002/chem.202301341 |
0.604 |
|
| 2023 |
Rohal RK, Banerjee D, Manchanda T, Bhardwaj V, Soma VR, Sankar M. Ethyl acetoacetate and acetylacetone appended hexabromo porphyrins: synthesis, spectral, electrochemical, and femtosecond third-order nonlinear optical studies. Dalton Transactions (Cambridge, England : 2003). PMID 37005971 DOI: 10.1039/d3dt00005b |
0.751 |
|
| 2023 |
Yadav I, Prakash V, Maurya MR, Sankar M. Oxido-Molybdenum(V) Corroles as Robust Catalysts for Oxidative Bromination and Selective Epoxidation Reactions in Aqueous Media under Mild Conditions. Inorganic Chemistry. 62: 5292-5301. PMID 36958040 DOI: 10.1021/acs.inorgchem.3c00504 |
0.635 |
|
| 2022 |
Yadav I, Shanu M, Acharyya JN, Prakash GV, Sankar M. Ultrafast Dynamics and Strong Two-Photon Absorption Properties of Nonplanar β-Functionalized "Push-Pull" Copper Corroles with a Mixed Substituent Pattern. Inorganic Chemistry. PMID 36403252 DOI: 10.1021/acs.inorgchem.2c03064 |
0.729 |
|
| 2022 |
Bulbul AS, Chaudhri N, Shanu M, Acharyya JN, Vijaya Prakash G, Sankar M. Unsymmetrically β-Functionalized π-Extended Porphyrins: Synthesis, Spectral, Electrochemical Redox Properties, and Their Utilization as Efficient Two-Photon Absorbers. Inorganic Chemistry. PMID 35729686 DOI: 10.1021/acs.inorgchem.2c00787 |
0.788 |
|
| 2022 |
Rohal RK, Shanu M, Acharyya JN, Vijaya Prakash G, Sankar M. Synthesis and the spectral, electrochemical, and nonlinear optical properties of β-dicyanovinyl-appended 'push-pull' porphyrins. Dalton Transactions (Cambridge, England : 2003). 51: 9049-9061. PMID 35642589 DOI: 10.1039/d2dt01016j |
0.773 |
|
| 2021 |
Rohal RK, Acharyya JN, Shanu M, Prakash GV, Sankar M. β-Tetracyanobutadiene-Appended Porphyrins: Facile Synthesis, Spectral and Electrochemical Redox Properties, and Their Utilization as Excellent Optical Limiters. Inorganic Chemistry. PMID 34882407 DOI: 10.1021/acs.inorgchem.1c02403 |
0.775 |
|
| 2021 |
Kumar S, Chaudhri N, Osterloh WR, Kadish KM, Sankar M. Nickel(II) monobenzoporphyrins and chlorins: synthesis, electrochemistry and anion sensing properties. Dalton Transactions (Cambridge, England : 2003). 50: 17086-17100. PMID 34779452 DOI: 10.1039/d1dt03122h |
0.425 |
|
| 2021 |
Kumar S, Acharyya JN, Banerjee D, Soma VR, Vijaya Prakash G, Sankar M. Strong two-photon absorption and ultrafast dynamics of -functionalized "push-pull" -ABC porphyrins. Dalton Transactions (Cambridge, England : 2003). PMID 33876809 DOI: 10.1039/d1dt00378j |
0.519 |
|
| 2020 |
Osterloh WR, Kumar S, Chaudhri N, Fang Y, Sankar M, Kadish KM. Facile Heterogeneous and Homogeneous Anion Induced Electrosynthesis: An Efficient Method for Obtaining π-Extended Porphyrins. Inorganic Chemistry. PMID 33143408 DOI: 10.1021/acs.inorgchem.0c02770 |
0.42 |
|
| 2020 |
Rathi P, Ekta, Kumar S, Banerjee D, Soma VR, Sankar M. Unsymmetrical β-functionalized 'push-pull' porphyrins: synthesis and photophysical, electrochemical and nonlinear optical properties. Dalton Transactions (Cambridge, England : 2003). PMID 32091509 DOI: 10.1039/c9dt04252k |
0.541 |
|
| 2019 |
Chaudhri N, Cong L, Bulbul AS, Grover N, Osterloh WR, Fang Y, Sankar M, Kadish KM. Structural, Photophysical, and Electrochemical Properties of Doubly Fused Porphyrins and Related Fused Chlorins. Inorganic Chemistry. PMID 31889445 DOI: 10.1021/Acs.Inorgchem.9B03329 |
0.743 |
|
| 2019 |
Cong L, Chahal MK, Osterloh R, Sankar M, Kadish KM. Synthesis, Electrochemistry, and Reversible Interconversion among Perhalogenated Hydroxyphenyl Ni(II) Porphyrins, Porphodimethenes, and Porpho-5,15-bis-paraquinone Methide. Inorganic Chemistry. 58: 14361-14376. PMID 31633340 DOI: 10.1021/Acs.Inorgchem.9B01642 |
0.351 |
|
| 2019 |
Rathi P, Butcher R, Sankar M. Unsymmetrical nonplanar 'push-pull' β-octasubstituted porphyrins: facile synthesis, structural, photophysical and electrochemical redox properties. Dalton Transactions (Cambridge, England : 2003). PMID 31556414 DOI: 10.1039/C9Dt02792K |
0.371 |
|
| 2019 |
D'Souza F, Prakash K, Alsaleh AZ, Rathi P, Sharma A, Sankar M. Synthesis, Spectral, Electrochemical and Photovoltaic Studies of A3B Porphyrinic Dyes having Peripheral Donors. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. PMID 31283866 DOI: 10.1002/Cphc.201900604 |
0.348 |
|
| 2019 |
Grover N, Chaudhri N, Sankar M. β-Functionalized Dibenzoporphyrins with Mixed Substituents Pattern: Facile Synthesis, Structural, Spectral, and Electrochemical Redox Properties. Inorganic Chemistry. PMID 30707015 DOI: 10.1021/acs.inorgchem.8b03106 |
0.393 |
|
| 2019 |
Sankar M, Bhyrappa P. Effect of solvent on the electronic absorption spectral properties of Ni(II) and Cu(II)-complexes of some mixed β-octasubstituted-meso-tetraphenylporphyrins Chemical Physics Letters. 730: 643-648. DOI: 10.1016/J.CPLETT.2019.06.053 |
0.716 |
|
| 2018 |
Chaudhri N, Cong L, Grover N, Shan W, Anshul K, Sankar M, Kadish KM. Synthesis and Electrochemical Characterization of Acetylacetone (acac) and Ethyl Acetate (EA) Appended β-Trisubstituted Push-Pull Porphyrins: Formation of Electronically Communicating Porphyrin Dimers. Inorganic Chemistry. 57: 13213-13224. PMID 30359002 DOI: 10.1021/Acs.Inorgchem.8B01690 |
0.404 |
|
| 2018 |
Chaudhri N, Grover N, Sankar M. Nickel-Induced Skeletal Rearrangement of Free Base trans-Chlorins into Monofused Ni-Porphyrins: Synthesis, Structural, Spectral, and Electrochemical Redox Properties. Inorganic Chemistry. PMID 30179467 DOI: 10.1021/acs.inorgchem.8b00798 |
0.407 |
|
| 2018 |
Chaudhri N, Grover N, Sankar M. Selective Conversion of Planar trans-Chlorins into Highly Twisted Doubly Fused Porphyrins or Chlorins via Oxidative Fusion. Inorganic Chemistry. PMID 29787261 DOI: 10.1021/acs.inorgchem.8b00849 |
0.399 |
|
| 2018 |
Ke X, Kumar R, Sankar M, Kadish KM. Electrochemistry and Spectroelectrochemistry of Cobalt Porphyrins with π-Extending and/or Highly Electron-Withdrawing Pyrrole Substituents. In Situ Electrogeneration of σ-Bonded Complexes. Inorganic Chemistry. PMID 29363959 DOI: 10.1021/Acs.Inorgchem.7B02856 |
0.397 |
|
| 2018 |
Bhyrappa P, Sankar M, Karunanithi K, Varghese B. Highly Nonplanar Macrocyclic Ring Conformation in the Crystal Structures of Ni(II) And Cu(II) Octaphenylporphyrins Journal of Structural Chemistry. 59: 415-424. DOI: 10.1134/S0022476618020233 |
0.673 |
|
| 2017 |
Bhyrappa P, Sankar M. Effect of solvent on the electronic absorption spectral properties of some mixed β-octasubstituted Zn(II)-tetraphenylporphyrins. Spectrochimica Acta. Part a, Molecular and Biomolecular Spectroscopy. 189: 80-85. PMID 28802858 DOI: 10.1016/j.saa.2017.07.059 |
0.652 |
|
| 2017 |
Yadav P, Sankar M, Ke X, Cong L, Kadish KM. Highly reducible π-extended copper corroles. Dalton Transactions (Cambridge, England : 2003). PMID 28726883 DOI: 10.1039/C7Dt01814B |
0.443 |
|
| 2017 |
Ke X, Yadav P, Cong L, Kumar R, Sankar M, Kadish KM. Facile and Reversible Electrogeneration of Porphyrin Trianions and Tetraanions in Nonaqueous Media. Inorganic Chemistry. PMID 28677964 DOI: 10.1021/Acs.Inorgchem.7B01262 |
0.471 |
|
| 2017 |
Rathi P, Chahal MK, Sankar M. Highly electron deficient tetrabenzoquinone-appended Ni(ii) and Cu(ii) porphyrins: spectral, solvatochromatic, electrochemical redox and tuneable F−and CN−sensing properties New Journal of Chemistry. 41: 11962-11968. DOI: 10.1039/C7NJ01866E |
0.363 |
|
| 2017 |
Yadav P, Kumar R, Saxena A, Butcher RJ, Sankar M. β-Trisubstituted “Push-Pull” Porphyrins - Synthesis and Structural, Photophysical, and Electrochemical Redox Properties European Journal of Inorganic Chemistry. 2017: 3269-3274. DOI: 10.1002/Ejic.201700310 |
0.305 |
|
| 2016 |
Grover N, Chaudhri N, Sankar M. Facile Conversion of Ni(II) Cyclopropylchlorins into Novel β-Substituted Porphyrins through Acid-Catalyzed Ring-Opening Reaction. Inorganic Chemistry. PMID 27991777 DOI: 10.1021/acs.inorgchem.6b02333 |
0.373 |
|
| 2016 |
Chahal MK, Sankar M. Switching between porphyrin, porphodimethene and porphyrinogen using cyanide and fluoride ions mimicking volatile molecular memory and the 'NOR' logic gate. Dalton Transactions (Cambridge, England : 2003). PMID 27711724 DOI: 10.1039/c6dt02506d |
0.355 |
|
| 2016 |
Dar TA, Chahal MK, Kumar RA, Sankar M. Synthesis, electrochemical and complexation studies of Zn(II) aryloxyporphyrins with fullerene C60 Journal of Porphyrins and Phthalocyanines. 20: 744-751. DOI: 10.1142/S1088424616500656 |
0.318 |
|
| 2015 |
Grover N, Sankar M, Song Y, Kadish KM. Asymmetrically Crowded "Push-Pull" Octaphenylporphyrins with Modulated Frontier Orbitals: Syntheses, Photophysical, and Electrochemical Redox Properties. Inorganic Chemistry. PMID 26716933 DOI: 10.1021/Acs.Inorgchem.5B01339 |
0.424 |
|
| 2015 |
Kumar R, Chaudhary N, Sankar M, Maurya MR. Electron deficient nonplanar β-octachlorovanadylporphyrin as a highly efficient and selective epoxidation catalyst for olefins. Dalton Transactions (Cambridge, England : 2003). 44: 17720-9. PMID 26394559 DOI: 10.1039/c5dt02349a |
0.357 |
|
| 2015 |
Grover N, Rathi P, Sankar M. Spectral investigations of meso-tetraalkylporphyrin-fullerene host–guest complexes Journal of Porphyrins and Phthalocyanines. 19: 997-1006. DOI: 10.1142/S1088424615500716 |
0.345 |
|
| 2015 |
Kumar R, Yadav P, Rathi P, Sankar M. Synthesis, spectroscopic, electrochemical redox, solvatochromism and anion binding properties of β-tetra- and -octaphenylethynyl substituted meso-tetraphenylporphyrins Rsc Advances. 5: 82237-82246. DOI: 10.1039/C5RA15211A |
0.34 |
|
| 2014 |
Kumar R, Sankar M. Synthesis, spectral, and electrochemical studies of electronically tunable β-substituted porphyrins with mixed substituent pattern. Inorganic Chemistry. 53: 12706-19. PMID 25412143 DOI: 10.1021/ic501259g |
0.381 |
|
| 2014 |
Yadav P, Sankar M. Synthesis, spectroscopic and electrochemical studies of phosphoryl and carbomethoxyphenyl substituted corroles, and their anion detection properties Dalton Transactions. 43: 14680-14688. PMID 25142377 DOI: 10.1039/c4dt01853b |
0.344 |
|
| 2013 |
Ishizuka T, Sankar M, Kojima T. Control of the spatial arrangements of supramolecular networks based on saddle-distorted porphyrins by intermolecular hydrogen bonding. Dalton Transactions (Cambridge, England : 2003). 42: 16073-9. PMID 23969510 DOI: 10.1039/c3dt51467f |
0.522 |
|
| 2013 |
Mongin O, Sankar M, Charlot M, Mir Y, Blanchard-Desce M. Strong enhancement of two-photon absorption properties in synergic ‘semi-disconnected’ multiporphyrin assemblies designed for combined imaging and photodynamic therapy Tetrahedron Letters. 54: 6474-6478. DOI: 10.1016/J.TETLET.2013.09.076 |
0.524 |
|
| 2012 |
Ishizuka T, Sankar M, Yamada Y, Fukuzumi S, Kojima T. Porphyrin nanochannels reinforced by hydrogen bonding. Chemical Communications (Cambridge, England). 48: 6481-3. PMID 22582178 DOI: 10.1039/C2Cc31142A |
0.451 |
|
| 2011 |
Sankar M, Ishizuka T, Wang Z, Ma T, Shiro M, Kojima T. Synthesis, structure and physicochemical properties of a saddle-distorted porphyrin with a peripheral carboxyl group Journal of Porphyrins and Phthalocyanines. 15: 421-432. DOI: 10.1142/S1088424611003379 |
0.557 |
|
| 2007 |
Bhyrappa P, Sankar M, Varghese B. Mixed substituted porphyrins: structural and electrochemical redox properties. Inorganic Chemistry. 45: 4136-49. PMID 16676974 DOI: 10.1021/IC052035B |
0.713 |
|
| 2006 |
Bhyrappa P, Sankar M, Varghese B, Bhavana P. meso-Tetrathienylporphyrins: Steady-state emission and structural properties Journal of Chemical Sciences. 118: 393-397. DOI: 10.1007/BF02711449 |
0.582 |
|
| 2005 |
Sankar M, Bhyrappa P, Varghese B, Praneeth KK, Vaijayanthimala G. Meso-tetrakis(3',5'-di-substituted-phenyl)porphyrins: structural, electrochemical redox and axial ligation properties Journal of Porphyrins and Phthalocyanines. 9: 413-422. DOI: 10.1142/S1088424605000514 |
0.722 |
|
| 2004 |
Sankar M, Arunkumar C, Bhyrappa P. Unusual solvent dependent electronic absorption spectral properties of nickel(II) and copper(II) perhaloporphyrins Journal of Porphyrins and Phthalocyanines. 8: 1343-1355. DOI: 10.1142/S1088424604000702 |
0.8 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2017 |
Prakash K, Manchanda S, Sudhakar V, Sharma N, Sankar M, Krishnamoorthy K. Facile synthesis of β-functionalized “push-pull” Zn(II) porphyrins for DSSC applications Dyes and Pigments. 147: 56-66. DOI: 10.1016/J.DYEPIG.2017.07.053 |
0.291 |
|
| 2017 |
Chaudhri N, Grover N, Sankar M. Versatile Synthetic Route for β-Functionalized Chlorins and Porphyrins by Varying the Size of Michael Donors: Syntheses, Photophysical, and Electrochemical Redox Properties. Inorganic Chemistry. PMID 28921964 DOI: 10.1021/acs.inorgchem.7b01158 |
0.289 |
|
| 2016 |
Kumar R, Saxena A, Sankar M. Mixed β-bromo/cyano tetrasubstituted-meso-tetraphenylporphyrin Cu(II) complexes: Synthesis and electrochemical studies Journal of Porphyrins and Phthalocyanines. 20: 1420-1425. DOI: 10.1142/S1088424616501169 |
0.288 |
|
| 2017 |
Chahal MK, Sankar M, Butcher RJ. An insight into the communication between β-olefin/phenyl olefin-mediated acceptors and porphyrin π-system: a way to establish porphyrin based chemodosimeters and chemosensors. Physical Chemistry Chemical Physics : Pccp. PMID 28124041 DOI: 10.1039/C6Cp08396J |
0.285 |
|
| 2018 |
Chaudhri N, Butcher RJ, Sankar M. Synthesis and structural, photophysical, electrochemical redox and axial ligation properties of highly electron deficient perchlorometalloporphyrins and selective CN− sensing by Co(ii) complexes New Journal of Chemistry. 42: 8190-8199. DOI: 10.1039/C7Nj04418F |
0.275 |
|
| 2015 |
Kumar R, Chaudhri N, Sankar M. Ratiometric and colorimetric "naked eye" selective detection of CN(-) ions by electron deficient Ni(II) porphyrins and their reversibility studies. Dalton Transactions (Cambridge, England : 2003). 44: 9149-57. PMID 25901694 DOI: 10.1039/c5dt00937e |
0.271 |
|
| 2020 |
Dar TA, Bulbul AS, Sankar M, Kadish KM. Meso-Tetrapyrenylporphyrins: Synthesis, structural, spectral, electrochemical properties and Förster energy transfer (FRET) studies Journal of Porphyrins and Phthalocyanines. 24: 985-992. DOI: 10.1142/S108842462050008X |
0.267 |
|
| 2017 |
Yadav P, Anand T, Moram SSB, Bhattacharya S, Sankar M, Rao SV. Synthesis and femtosecond third order nonlinear optical properties of push-pull trans- A 2 B-corroles Dyes and Pigments. 143: 324-330. DOI: 10.1016/J.DYEPIG.2017.04.041 |
0.266 |
|
| 2016 |
Kumar R, Sankar M, Sudhakar V, Krishnamoorthy K. Synthesis and characterization of simple cost-effective trans-A2BC porphyrins with various donor groups for dye-sensitized solar cells New Journal of Chemistry. 40: 5704-5713. DOI: 10.1039/C5NJ02610E |
0.266 |
|
| 2020 |
Yadav M, Sonkar PK, Prakash K, Ganesan V, Sankar M, Yadav DK, Gupta R. Insight into efficient bifunctional catalysis: Oxygen reduction and oxygen evolution reactions using MWCNTs based composites with 5,10,15,20-tetrakis(3′,5′-dimethoxyphenyl)porphyrinato cobalt(II) and 5,10,15,20-tetrakis(3′,5′-dihydroxyphenyl)porphyrinato cobalt(II) International Journal of Hydrogen Energy. 45: 9710-9722. DOI: 10.1016/j.ijhydene.2020.01.224 |
0.265 |
|
| 2023 |
Maurya MR, Prakash V, Dar TA, Sankar M. Facile Synthesis of β-Tetracyano Vanadyl Porphyrin from Its Tetrabromo Analogue and Its Excellent Catalytic Activity for Bromination and Epoxidation Reactions. Acs Omega. 8: 6391-6401. PMID 36844578 DOI: 10.1021/acsomega.2c06638 |
0.263 |
|
| 2017 |
Yadav P, Rathi P, Sankar M. Facile Generation of AB Corrole Radical Using Fe(III) Salts and Its Spectroscopic Properties. Acs Omega. 2: 959-965. PMID 30023622 DOI: 10.1021/acsomega.6b00430 |
0.262 |
|
| 2020 |
Dar TA, Sankar M. Fused Nickel(II) Porphyrins-Sensing of Toxic Anions and Selected Metal Ions Through Supramolecular Interactions. Frontiers in Chemistry. 8: 595177. PMID 33282838 DOI: 10.3389/fchem.2020.595177 |
0.261 |
|
| 2015 |
Chaudhri N, Grover N, Sankar M. Asymmetrically β-substituted porphyrins and chlorins: Synthesis, spectroscopic and electrochemical redox properties Ecs Transactions. 66: 11-20. DOI: 10.1149/06616.0011ecst |
0.258 |
|
| 2020 |
Sankar M, Rathi P, Ganesan A, Seetharaman S, Karr PA, D'Souza F. A Persubstituted Triphenylamine Bearing Dendritic Zinc Porphyrin to Host Endohedral Fullerene, ScN@C: Formation and Excited State Electron Transfer. The Journal of Physical Chemistry. B. PMID 32525676 DOI: 10.1021/acs.jpcb.0c04392 |
0.252 |
|
| 2019 |
Prakash K, Sudhakar V, Sankar M, Krishnamoorthy K. Trans-A2B2 Zn(II) porphyrin dyes with various donor groups and their Co-sensitization for highly efficient dye-sensitized solar cells Dyes and Pigments. 160: 386-394. DOI: 10.1016/J.DYEPIG.2018.08.029 |
0.25 |
|
| 2015 |
Prakash K, Kumar R, Sankar M. Mono- and tri-β-substituted unsymmetrical metalloporphyrins: synthesis, structural, spectral and electrochemical properties Rsc Advances. 5: 66824-66832. DOI: 10.1039/c5ra12711d |
0.248 |
|
| 2017 |
Chahal MK, Sankar M. β-Dicyanovinyl substituted porphyrinogen: synthesis, a reversible sensor for picric acid among explosives and a unique sensor for cyanide and fluoride ions by switching between various porphyrinoid states. Dalton Transactions (Cambridge, England : 2003). PMID 28792058 DOI: 10.1039/c7dt01158j |
0.241 |
|
| 2019 |
Dar TA, Tomar R, Mian RM, Sankar M, Maurya MR. Vanadyl β-tetrabromoporphyrin: synthesis, crystal structure and its use as an efficient and selective catalyst for olefin epoxidation in aqueous medium. Rsc Advances. 9: 10405-10413. PMID 35520888 DOI: 10.1039/c8ra09825e |
0.236 |
|
| 2018 |
Grover N, Kumar R, Chaudhri N, Butcher R, Sankar M. β-Heptasubstituted Porphyrins: Synthesis, Structural, Spectral, and Electrochemical Properties European Journal of Inorganic Chemistry. 2018: 3338-3343. DOI: 10.1002/Ejic.201800410 |
0.235 |
|
| 2019 |
Dar TA, Tomar R, Mian RM, Sankar M, Maurya MR. Vanadyl β-tetrabromoporphyrin: synthesis, crystal structure and its use as an efficient and selective catalyst for olefin epoxidation in aqueous medium Rsc Advances. 9: 10405-10413. DOI: 10.1039/C8Ra09825E |
0.23 |
|
| 2020 |
Grover N, Sankar M. N-Confused Porphyrin - A Unique "Turn-On" Chemosensor for CN and F ions and "Turn-Off" Sensor for ClO ions. Chemistry, An Asian Journal. PMID 32468689 DOI: 10.1002/asia.202000557 |
0.223 |
|
| 2017 |
Yadav P, Sankar M. Facile synthesis, photophysical and electrochemical redox properties of octa- and tetracarboxamidophenylporphyrins and the first example of amido-imidol tautomerism in porphyrins Dyes and Pigments. 139: 651-657. DOI: 10.1016/J.DYEPIG.2016.10.053 |
0.22 |
|
| 2015 |
Kumar R, Yadav P, Kumar A, Sankar M. Facile Synthesis and Electrochemical Studies of Diethoxyphosphorylphenyl-substituted Porphyrin and Its Metal Complexes Chemistry Letters. 44: 914-916. DOI: 10.1246/Cl.150233 |
0.217 |
|
| 2020 |
Osterloh WR, Fang Y, Chaudhri N, Cong L, Sankar M, Kadish KM. Effect of fused indanedione (IND) groups and antipodal β-substituents on electrochemical properties of unsymmetrical metalloporphyrins Journal of Porphyrins and Phthalocyanines. DOI: 10.1142/S108842462050039X |
0.213 |
|
| 2019 |
Grover N, Chaudhri N, Sankar M. β-substituted donor-acceptor porphyrins: Synthesis, energy transfer and electrochemical redox properties Dyes and Pigments. 161: 104-112. DOI: 10.1016/J.DYEPIG.2018.09.028 |
0.209 |
|
| 2015 |
Chahal MK, Sankar M. Porphyrin chemodosimeters: synthesis, electrochemical redox properties and selective ‘naked-eye’ detection of cyanide ions Rsc Advances. 5: 99028-99036. DOI: 10.1039/C5RA19847J |
0.193 |
|
| 2022 |
Jha A, Shankar H, Kumar S, Sankar M, Kar P. Efficient charge transfer from organometal lead halide perovskite nanocrystals to free base -tetraphenylporphyrins. Nanoscale Advances. 4: 1779-1785. PMID 36132160 DOI: 10.1039/d1na00835h |
0.191 |
|
| 2019 |
Dar TA, Uprety B, Sankar M, Maurya MR. Robust and electron deficient oxidovanadium(iv) porphyrin catalysts for selective epoxidation and oxidative bromination reactions in aqueous media Green Chemistry. 21: 1757-1768. DOI: 10.1039/C8GC03909G |
0.19 |
|
| 2017 |
Chaudhri N, Sawhney N, Madhusudhan B, Raghav A, Sankar M, Satapathi S. Effect of functional groups on sensitization of dye-sensitized solar cells (DSSCs) using free base porphyrins Journal of Porphyrins and Phthalocyanines. 21: 222-230. DOI: 10.1142/S1088424617500390 |
0.189 |
|
| 2020 |
Anand T, Sankar M. A dual colorimetric chemosensor for Hg(II) and cyanide ions in aqueous media based on a nitrobenzoxadiazole (NBD)-antipyrine conjugate with INHIBIT logic gate behaviour. Analytical Methods : Advancing Methods and Applications. PMID 32929433 DOI: 10.1039/d0ay00913j |
0.189 |
|
| 2018 |
Sonkar PK, Yadav M, Prakash K, Ganesan V, Sankar M, Yadav DK, Gupta R. Electrochemical sensing of rifampicin in pharmaceutical samples using meso-tetrakis(4-hydroxyphenyl)porphyrinato cobalt(II) anchored carbon nanotubes Journal of Applied Electrochemistry. 48: 937-946. DOI: 10.1007/s10800-018-1221-3 |
0.188 |
|
| 2021 |
Maurya MR, Prakash V, Avecilla F, Sankar M. Selective Bromination of
β
‐Positions of Porphyrin by Self‐Catalytic Behaviour of VOTPP: Facile Synthesis, Electrochemical Redox Properties and Catalytic Application European Journal of Inorganic Chemistry. 2021: 1685-1694. DOI: 10.1002/EJIC.202100116 |
0.187 |
|
| 2020 |
Tripathi D, Yadav I, Negi H, Singh RK, Srivastava VC, Sankar M. Highly efficient Co(II) porphyrin catalysts for the extractive oxidative desulfurization of dibenzothiophene in fuel oils under mild conditions Journal of Porphyrins and Phthalocyanines. 25: 24-30. DOI: 10.1142/s1088424620500443 |
0.168 |
|
| 2017 |
Sonkar PK, Prakash K, Yadav M, Ganesan V, Sankar M, Gupta R, Yadav DK. Co(ii)-porphyrin-decorated carbon nanotubes as catalysts for oxygen reduction reactions: an approach for fuel cell improvement Journal of Materials Chemistry A. 5: 6263-6276. DOI: 10.1039/C6TA10482G |
0.166 |
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| 2020 |
Fang Y, Yadav I, Osterloh WR, Chaudhri N, Sankar M, Kadish KM. Electrochemistry of Tri‐substituted Porphyrins with
β
‐Appended Ethyl Acetoacetate and Acetylacetone in Neutral and Basic Nonaqueous Solvents Chemelectrochem. 7: 1723-1732. DOI: 10.1002/celc.202000191 |
0.162 |
|
| 2017 |
Sah U, Sharma K, Chaudhri N, Sankar M, Gopinath P. Antimicrobial photodynamic therapy: Single-walled carbon nanotube (SWCNT)-Porphyrin conjugate for visible light mediated inactivation of Staphylococcus aureus. Colloids and Surfaces. B, Biointerfaces. 162: 108-117. PMID 29190461 DOI: 10.1016/j.colsurfb.2017.11.046 |
0.158 |
|
| 2018 |
Kumar R, Sudhakar V, Prakash K, Krishnamoorthy K, Sankar M. Tuning the Photovoltaic Performance of DSSCs by Appending Various Donor Groups on trans-Dimesityl Porphyrin Backbone Acs Applied Energy Materials. 1: 2793-2801. DOI: 10.1021/ACSAEM.8B00458 |
0.151 |
|
| 2017 |
Prakash K, Sankar M. Borylated porphyrin and its metal complexes: Synthesis, electrochemistry and deprotection-protection strategy for anion sensing Sensors and Actuators B: Chemical. 240: 709-717. DOI: 10.1016/J.SNB.2016.09.016 |
0.15 |
|
| 2017 |
Yadav P, Sankar M. Spectroscopic and theoretical studies of anionic corroles derived from phosphoryl and carbomethoxyphenyl substituted corroles Chemical Physics Letters. 677: 107-113. DOI: 10.1016/J.CPLETT.2017.04.011 |
0.148 |
|
| 2024 |
Rohal RK, Banerjee D, Rana N, Soma VR, Sankar M. Third-order nonlinear optical properties of highly electron deficient, nonplanar push-pull porphyrins: β-nitro-hexa-substituted porphyrins bearing bromo, phenyl, and phenylethynyl groups. Dalton Transactions (Cambridge, England : 2003). PMID 38506309 DOI: 10.1039/d4dt00045e |
0.12 |
|
| 2024 |
Bulbul AS, Rathour V, Ganesan V, Sankar M. π-Extended nonplanar cobalt porphyrins immobilized on MWCNTs as efficient electrocatalysts for selective oxygen reduction reaction. Chemical Communications (Cambridge, England). 60: 3146-3149. PMID 38348482 DOI: 10.1039/d3cc05803d |
0.12 |
|
| 2015 |
Chahal MK, Sankar M. 1,8-Naphthyridinic fluorescent ‘turn-on’ and ‘turn-off’ chemosensors for detection of F−and Hg2+ions mimicking INHIBIT molecular logic behaviour Analytical Methods. 7: 4552-4559. DOI: 10.1039/C5AY00752F |
0.103 |
|
| 2015 |
Chaudhri N, Sankar M. Colorimetric "naked eye" detection of CN-, F-, CH3COO- and H2PO4 - ions by highly nonplanar electron deficient perhaloporphyrins Rsc Advances. 5: 3269-3275. DOI: 10.1039/c4ra11368c |
0.095 |
|
| 2018 |
Chahal MK, Dar TA, Sankar M. Facile synthesis of functionalized urea, imidazolium salt, azide, and triazole from a 2-amino-5,7-dimethyl-1,8-naphthyridine scaffold and their utilization in fluoride ion sensing New Journal of Chemistry. 42: 10059-10066. DOI: 10.1039/C8NJ00503F |
0.087 |
|
| 2015 |
Chahal MK, Sankar M. 1,8-Naphthyridine-based fluorescent receptors for picric acid detection in aqueous media Analytical Methods. 7: 10272-10279. DOI: 10.1039/C5AY01464F |
0.077 |
|
| 2017 |
Dar TA, Sankar M. Facile Synthesis of Nitrovanillin- Appended Porphyrin and Its Utilization as Potent, Recyclable, Naked-Eye CN−and F−Ion Sensor Chemistryselect. 2: 6778-6783. DOI: 10.1002/SLCT.201701222 |
0.052 |
|
| 2023 |
Shukla A, Kumari S, Sankar M, Nair MS. Insights into the mechanism of binding of doxorubicin and a chlorin compound with 22-mer c-Myc G quadruplex. Biochimica Et Biophysica Acta. General Subjects. 1867: 130482. PMID 37821013 DOI: 10.1016/j.bbagen.2023.130482 |
0.051 |
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