Year |
Citation |
Score |
2024 |
Tasleem M, Singh V, Tiwari A, Ganesan V, Sankar M. Electrocatalysis Using Cobalt Porphyrin Covalently Linked with Multi-Walled Carbon Nanotubes: Hydrazine Sensing and Hydrazine-Assisted Green Hydrogen Synthesis. Small (Weinheim An Der Bergstrasse, Germany). e2401273. PMID 38958069 DOI: 10.1002/smll.202401273 |
0.778 |
|
2024 |
Yadav SK, Patter A, Sankar M. Enhanced Catalytic Activity of Binuclear Oxidovanadium(IV) Bisbenzimidazole Linked Porphyrin Dimer for the Generation of Biologically Active 3,4-Dihydropyrimidinones and Their Corresponding Thiones. Inorganic Chemistry. 63: 11102-11112. PMID 38831586 DOI: 10.1021/acs.inorgchem.4c00701 |
0.576 |
|
2024 |
Yadav I, Acharyya JN, Prakash GV, Sankar M. Structurally influenced optical nonlinearities and ultrafast dynamics in β-acroleyl- and β-dicyanobutadienyl-appended cobalt corroles. Physical Chemistry Chemical Physics : Pccp. PMID 38764422 DOI: 10.1039/d4cp00090k |
0.663 |
|
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 |
0.757 |
|
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 |
0.754 |
|
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 |
0.678 |
|
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 |
0.347 |
|
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 |
0.775 |
|
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 |
0.677 |
|
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 |
0.6 |
|
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 |
0.782 |
|
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 |
0.638 |
|
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 |
0.727 |
|
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 |
0.81 |
|
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 |
0.8 |
|
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 |
0.802 |
|
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 |
0.383 |
|
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 |
0.49 |
|
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 |
0.384 |
|
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 |
0.518 |
|
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 |
0.765 |
|
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 |
0.32 |
|
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 |
0.348 |
|
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 |
0.324 |
|
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 |
0.371 |
|
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 |
0.698 |
|
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 |
0.365 |
|
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 |
0.369 |
|
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 |
0.379 |
|
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 |
0.366 |
|
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 |
0.653 |
|
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 |
0.648 |
|
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 |
0.394 |
|
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 |
0.425 |
|
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 |
0.324 |
|
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 |
0.345 |
|
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 |
0.316 |
|
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 |
0.384 |
|
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 |
0.337 |
|
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 |
0.31 |
|
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 |
0.318 |
|
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 |
0.35 |
|
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 |
0.315 |
|
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 |
0.511 |
|
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 |
0.529 |
|
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 |
0.45 |
|
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 |
0.546 |
|
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 |
0.701 |
|
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 |
0.578 |
|
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 |
0.703 |
|
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 |
0.795 |
|
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