Selected Publications
(Aug 2014 to Dec 2023)
67. Yadav, I., & Sankar, M*. (2023). Panchromatic and Perturbed Absorption Spectral Features and Multiredox Properties of Dicyanovinyl- and Dicyanobutadienyl-Appended Cobalt Corroles. Inorganic Chemistry, 62. https://doi.org/10.1021/ACS.INORGCHEM.3C02666
66. Shukla, A., Kumari, S., Sankar, M*., & Nair, M. S. (2023). Insights into the mechanism of binding of doxorubicin and a chlorin compound with 22-mer c-Myc G quadruplex. Biochimica et Biophysica Acta (BBA) - General Subjects, 1867(12), 130482. https://doi.org/10.1016/J.BBAGEN.2023.130482
65. I. Yadav, V. Prakash, R.R. Kaswan, M.R. Maurya, M. Sankar*, Highly Efficient β-Functionalized Oxidomolybdenum(V) Corroles for Catalytic Oxidative Bromination of Phenols at Room Temperature, Eur J Inorg Chem. (2023) e202300459. https://doi.org/10.1002/EJIC.202300459.
64. M.R. Maurya, V. Prakash, I. Yadav, M. Sankar,* Effect of para-Substituents on meso-Functionalized Oxidovanadium(IV) Porphyrins as Catalysts for Oxygen Atom Transfer Mediated Oxidation of Benzoin to Benzil under Mild Conditions, Eur J Inorg Chem. (2023) e202300374. https://doi.org/10.1002/EJIC.202300374.
63. S. Kumari, I. Yadav, J.N. Acharyya, M. Shanu, G.V. Prakash, M. Sankar*, Push–pull octaphenylporphyrins with mixed substituents pattern: Synthesis, redox, ultrafast dynamics and nonlinear optical studies, Dye. Pigment. 217 (2023) 111416. https://doi.org/10.1016/j.dyepig.2023.111416.
62. M. Tasleem, M. Yadav, V. Ganesan, M. Sankar*, Co(II) Porphyrin-MWCNT Nanoconjugate as an Efficient and Durable Electrocatalyst for Oxygen Reduction Reaction, Langmuir. 39 (2023) 8075–8082. https://doi.org/10.1021/ACS.LANGMUIR.3C00380.
61. I. Yadav, W.R. Osterloh, K.M. Kadish, M. Sankar*, Synthesis, Spectral, Redox, and Sensing Studies of β-Dicyanovinyl-Appended Corroles and Their Metal Complexes, Inorg. Chem. 62 (2023) 7738–7752. https://doi.org/10.1021/ACS.INORGCHEM.3C00341.
60. I. Yadav, J.K. Sharma, M. Sankar, F.D.’ Souza, F. D’souza, I. Yadav, M. Sankar*, ] J K Sharma, F. D’souza, Symmetrically Functionalized Copper and Silver Corrole-Bis-Tetracyanobutadiene Push-Pull Conjugates: Efficient Population of Triplet States via Charge Transfer, Chem. – A Eur. J. (2023) e202301341. https://doi.org/10.1002/CHEM.202301341.
59. I. Yadav, V. Prakash, M.R. Maurya, M. Sankar*, Oxido-Molybdenum(V) Corroles as Robust Catalysts for Oxidative Bromination and Selective Epoxidation Reactions in Aqueous Media under Mild Conditions, Inorg. Chem. 62 (2023) 5292–5301. https://doi.org/10.1021/acs.inorgchem.3c00504.
58. M.R. Maurya, V. Prakash, T.A. Dar, M. Sankar*, Facile Synthesis of β-Tetracyano Vanadyl Porphyrin from Its Tetrabromo Analogue and Its Excellent Catalytic Activity for Bromination and Epoxidation Reactions, ACS Omega. 8 (2023) 6391–6401. https://doi.org/10.1021/acsomega.2c06638.
57. R.K. Rohal, D. Banerjee, T. Manchanda, V. Bhardwaj, V.R. Soma, M. Sankar*, Ethyl Acetoacetate and Acetylacetone Appended Hexabromo Porphyrins: Synthesis, Spectral, Electrochemical, and Femtosecond Third-Order Nonlinear Optical Studies, Dalt. Trans. 52 (2023) 5523–5533. https://doi.org/10.1039/d3dt00005b.
56. I. Yadav, M. Shanu, J.N. Acharyya, G.V. Prakash, M. Sankar*, Ultrafast Dynamics and Strong Two-Photon Absorption Properties of Nonplanar β-Functionalized “Push-Pull” Copper Corroles with a Mixed Substituent Pattern, Inorg Chem. 2022 (2022) 61. https://doi.org/10.1021/ACS.INORGCHEM.2C03064/ASSET/IMAGES/LARGE/IC2C03064_0010.JPEG.
55. K. Prakash, M. Sankar*, β-Diformyl porphyrins: Synthesis, structural, spectral and electrochemical properties, J Porphyr Phthalocyanines. 26 (2022) 862–871. https://doi.org/10.1142/S1088424622500729.
54. P. Rathi, K. Prakash, M. Sankar*, β-Functionalized palladium(II) porphyrins: Facile synthesis, structural, spectral, and electrochemical redox properties, J Porphyr Phthalocyanines. (2022) A-H. https://doi.org/10.1142/S1088424622500845.
53. A.S. Bulbul, N. Chaudhri, M. Shanu, J.N. Acharyya, G. Vijaya Prakash, M. Sankar*, Unsymmetrically β-Functionalized π-Extended Porphyrins: Synthesis, Spectral, Electrochemical Redox Properties, and Their Utilization as Efficient Two-Photon Absorbers, Inorganic Chemistry. (2022). https://doi.org/10.1021/acs.inorgchem.2c00787.
52. V. Singh, P.S. Thakur, V. Ganesan, M. Sankar*, Zn(II) porphyrin-based polymer facilitated electrochemical synthesis of green hydrogen peroxide, Journal of Electroanalytical Chemistry. (2022) 116536. https://doi.org/10.1016/j.jelechem.2022.116536.
51. R.K. Rohal, M. Shanu, J.N. Acharyya, G. Vijaya Prakash, M. Sankar*, Synthesis and the spectral, electrochemical, and nonlinear optical properties of β-dicyanovinyl-appended ‘push–pull’ porphyrins, Dalton Transactions. 51 (2022) 9049–9061. https://doi.org/10.1039/D2DT01016J.
50. A. Jha, H. Shankar, S. Kumar, M. Sankar*, P. Kar, Efficient charge transfer from organometal lead halide perovskite nanocrystals to free base meso -tetraphenylporphyrins, Nanoscale Advances. 4 (2022) 1779–1785. https://doi.org/10.1039/D1NA00835H.
49. P.S. Thakur, M. Sankar*, Nanobiosensors for Biomedical, Environmental, and Food Monitoring Applications, Mater. Lett. 311 (2021) 131540. https://doi.org/10.1016/j.matlet.2021.131540
48. R.K. Rohal, J.N. Acharyya, M. Shanu, G.V. Prakash, M. Sankar*, β-Tetracyanobutadiene-Appended Porphyrins: Facile Synthesis, Spectral, and Electrochemical Redox Properties, and Their Utilization as Excellent Optical Limiters, Inorg. Chem. (2021). https://doi.org/10.1021/acs.inorgchem.1c02403 (Highlighted on the cover of the journal).
47. S. Kumar, N. Chaudhri, W.R. Osterloh, K.M. Kadish, M. Sankar*, Nickel(ii) monobenzoporphyrins and chlorins: synthesis, electrochemistry, and anion sensing properties, Dalt. Trans. 50 (2021) 17086–17100. https://doi.org/10.1039/d1dt03122h.
46. K. Prakash, W.R. Osterloh, P. Rathi, K.M. Kadish, M. Sankar*, Facile synthesis of antipodal β-arylaminodibromoporphyrins through Buchwald-Hartwig C-N coupling reaction and exploring their spectral and electrochemical redox properties, J. Organomet. Chem. 956 (2021)122114. https://doi.org/10.1016/j.jorganchem.2021.122114.
45. M.R. Maurya, V. Prakash, M. Sankar*, Selective epoxidation of olefins by vanadylporphyrin [V(IV)O(TPP)] and electron-deficient nonplanar β-octabromovanadylporphyrin [V(IV)O(TPPBr8)], J. Porphyr. Phthalocyanines. 1088424622020023 (2021) 1–8. https://doi.org/10.1142/s108842462250002x.
doi.org/10.1002/ejic.202100116
43. I Yadav, D Dhiman, M Sankar*, "β-Disubstituted silver (III) corroles: Facile synthesis, photophysical and electrochemical redox properties" Journal of Porphyrins and Phthalocyanines, 2021,547-554. https://doi.org/10.1142/S1088424621500437
(Invited Article on the occasion of 65th Birthday of Prof. T. K. Chandrashekar).
42. S Kumar, JN Acharyya, D Banerjee, VR Soma, GV Prakash, S Muniappan*, "Strong Two-photon Absorption and Ultrafast Dynamics in Meso-Functionalized‟ Push-Pull” Trans-A2BC Porphyrins" Dalton Trans., 2021,50, 6256-6272. https://doi.org/10.1039/D1DT00378J
41. D Tripathi, I Yadav, H Negi, RK Singh, VC Srivastava, M Sankar*, "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 (01),2021,24-30.
https://doi.org/10.1142/S1088424620500443
40. TA Dar, M Sankar*, "Fused Nickel (II) Porphyrins—Sensing of Toxic Anions and Selected Metal Ions Through Supramolecular Interactions" Frontiers in chemistry 8, 1050. https://doi.org/10.3389/fchem.2020.595177
39. WR Osterloh, S Kumar, N Chaudhri, Y Fang, M Sankar*, KM Kadish "Facile Heterogeneous and Homogeneous Anion Induced Electrosynthesis: An Efficient Method for Obtaining π-Extended Porphyrins" Inorganic Chemistry 59 (22), 2021,16737-16746.
https://doi.org/10.1021/acs.inorgchem.0c02770
38. T. Anand and M. Sankar*, “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” Anal. Methods 2020, 12, 4526-4533 (Highlighted on the cover of the journal). doi.org/10.1039/D0AY00913J
37. M. Sankar*, P. Rathi, A. Ganesan, S. Seetharaman, P. A. Karr and F. D'Souza “A Persubstituted Triphenylamine Bearing Dendritic Zinc Porphyrin to Host Endohedral Fullerene, Sc3N@C80: Formation and Excited State Electron Transfer”, J. Phys. Chem. B 2020, 124. https://pubs.acs.org/doi/10.1021/acs.jpcb.0c04392
36. N. Grover and M. Sankar*, “N-Confused Porphyrin - A Unique "Turn-on” Chemosensor for F- and CN- ions and "Turn off" for ClO4- ions, Chem. Asian J. 2020,15. https://doi.org/10.1002/asia.202000557
35. P. Rathi, Ekta, S. Kumar, D. Banerjee, S. V. Rao and M. Sankar*, “Unsymmetrical β-Functionalized ‘Push-Pull’ Porphyrins: Synthesis, Photophysical, Electrochemical and Nonlinear Optical Properties”, Dalton Trans. 2020, 49, 3198-3208. https://pubs.rsc.org/en/content/articlelanding/2020/dt/c9dt04252k#!divAbstract
34. N. Chaudhri, L. Cong, A. S. Bulbul, N. Grover, W. R. Osterloh, Y. Fang, M. Sankar* and K. M. Kadish, “Structural, Photophysical, and Electrochemical Properties of Doubly Fused Porphyrins and Related Fused Chlorins”, Inorg. Chem. 2020, 59, 1481-1495. https://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.9b03329
33. N. Grover, N. Chaudhri and M. Sankar*, “β-Functionalized Dibenzoporphyrins with Mixed Substitutents Pattern: Facile Synthesis, Structural, Spectral and Electrochemical Redox Properties”, Inorg. Chem. 2019, 58, 2514-2522. https://pubs.acs.org/doi/10.1021/acs.inorgchem.8b03106
32. P. Rathi, R. Butcher and M. Sankar*, “Unsymmetrical Nonplanar ‘Push-Pull’ β-Octa-substituted Porphyrins: Facile Synthesis, Structural, Photophysical and Electrochemical Redox Properties”, Dalton Trans. 2019, 48, 15002-15011 (Highlighted in the back cover of the journal). https://pubs.rsc.org/en/content/articlelanding/2019/dt/c9dt02792k#!divAbstract
31. L. Cong§, M. K. Chahal§, R. Osterloh, M. Sankar* and K. M. Kadish, “Synthesis, Electrochemistry, and Reversible Interconversion among Perhalogenated Hydroxyphenyl Ni(II) Porphyrins, Porphodimethenes, and Porpho-5,15-bis-paraquinone Methide”, Inorg. Chem. 2019, 58, 14361-14376 (§these authors contributed equally to this work). https://pubs.acs.org/doi/10.1021/acs.inorgchem.9b01642
30. T. A. Dar, B. Uprety, M. Sankar* and M. R. Maurya, “Robust and Electron Deficient Oxidovanadium(IV) Porphyrin Catalyst for Selective Epoxidation and Oxidative Bromination Reactions in Aqueous Media”, Green Chem. 2019, 21, 1757-1768. https://pubs.rsc.org/en/content/articlelanding/2019/gc/c8gc03909g#!divAbstract
29. K. Prakash, A. Z. Alsaleh, Neeraj, P. Rathi, A. Sharma, M. Sankar* and F. D’Souza, “Synthesis, Spectral, Electrochemical and Photovoltaic Studies of A3B Porphyrinic Dyes having Peripheral Donors”, ChemPhysChem 2019, 20, 2627-2634 (Invited article for the Special Issue on Solar Cells). https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cphc.201900604
28. K. Prakash, M. Sankar*, S. Seetharaman, and F. D’Souza, “Synthesis, Electrochemical and Photochemical Studies on π-Extended Mono-β-Functionalized Porphyrin Dyads”, ChemPhotoChem. 2019, 3, 151-165.
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cptc.201800165
27. K. Prakash, V. Sudhakar, K. Krishnamoorthy and M. Sankar*, “Trans-A2B2 Zn(II)-Porphyrin Dyes with Various Donor Groups and their Co-sensitization for Highly Efficient Dye-Sensitized Solar Cells”, Dyes Pigm. 2019, 160, 386-394.
https://www.sciencedirect.com/science/article/abs/pii/S0143720818306685
26. N. Chaudhri, L. Cong, N. Grover, W. Shan, K. Ansul, M. Sankar* and K. M. Kadish, “Synthesis and Electrochemical Characterization of Acetylacetone (acac) and Ethyl Acetate (EA) Appended β-Trisubstituted Push-Pull Porphyrins: Formation of Electronically Communicating Porphyrin Dimers”, Inorg. Chem. 2018, 57, 13213-13224. https://pubs.acs.org/doi/10.1021/acs.inorgchem.8b01690
25. R. Kumar, V. Sudhakar, K. Prakash, K. Krishnamoorthy and M. Sankar*, “Tuning the Photovoltaic Performance of DSSCs by Appending Various Donor Groups on Trans-Dimesityl Porphyrin Backbone”, ACS Appl. Energy Mater. 2018, 1, 2793-2801 (One of the Most Read articles during May-July 2018). https://pubs.acs.org/doi/10.1021/acsaem.8b00458
24. N. Chaudhri, N. Grover and M. Sankar*, “Nickel Induced Skeletal Rearrangement of Free Base trans-Chlorins into Monofused Ni(II)-Porphyrins: Synthesis, Structural, Spectral and Electrochemical Redox Properties”, Inorg. Chem. 2018, 57, 11349-11360.
https://pubs.acs.org/doi/10.1021/acs.inorgchem.8b00798
23. N. Chaudhri, N. Grover and M. Sankar*, “Selective Conversion of Planar trans-Chlorins into Highly Twisted Doubly Fused-Porphyrins or -Chlorins via Oxidative Fusion”, Inorg. Chem. 2018, 57, 6658-6668. https://pubs.acs.org/doi/10.1021/acs.inorgchem.8b00849
22. X. Ke, R. Kumar, M. Sankar* and K. M. Kadish, “Electrochemistry and Spectroelectrochemistry of Cobalt Porphyrins with π-Extending and/or Highly Electron-Withdrawing Pyrrole Substituents. In Situ Electrogeneration of σ-Bonded Complexes”, Inorg. Chem. 2018, 57, 1490-1503. https://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.7b02856
21. N. Chaudhri, R. J. Butcher and M. Sankar*, “Synthesis, Structural, Photophysical, Electrochemical Redox and Axial Ligation Properties of Highly Electron Deficient Perchlorometalloporphyrins and Selective CN– Sensing by Co(II) Complexes”, New J. Chem. 2018, 42, 8190-8199 (Invited article for the themed issue on Equilibrium Solution Coordination Chemistry).
https://pubs.rsc.org/en/content/articlelanding/2018/nj/c7nj04418f#!divAbstract
20. M. K. Chahal, T. A. Dar and M. Sankar*, “Facile Synthesis of Functionalized Urea, Imidazolium Salt, Azide and Triazole from 2-Amino-5,7-Dimethyl-1,8-Naphthyridine Scaffold and their Utilization in Fluoride ion Sensing”, New J. Chem. 2018, 42, 10059-10066. https://pubs.rsc.org/en/content/articlelanding/2018/nj/c8nj00503f#!divAbstract
19. P. K. Sonkar, M. Yadav, K. Prakash, V. Ganesan, M. Sankar*, D. K. Yadav and R. Gupta, “Electrochemical sensing of rifampicin in pharmaceutical samples using meso-tetrakis(4-hydroxyphenyl)porphyrinatocobalt(II) anchored carbon nanotubes”, J. Appl. Electrochem. 2018, 48, 937-946.
18. N. Chaudhri, N. Grover and M. Sankar*, “Versatile Synthetic Route for β-Functionalized Chlorins and Porphyrins by Varying the Size of Michael Donors: Syntheses, Photophysical & Electrochemical Redox Properties”, Inorg. Chem. 2017, 56, 11532-11542 (Highlighted at ACS Inorg. Chem. journal site as HOT paper). https://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.7b01158
17. M. K. Chahal and M. Sankar*, “β-Dicyanovinyl Substituted Porphyrinogen: Synthesis, Reversible Sensor for Picric Acid among Explosives and Unique Sensor for Cyanide and Fluoride ions by Switching between Various Porphyrinoid States”, Dalton Trans. 2017, 46, 11669-11678 (Highlighted by RSTV and leading Newspapers in India).
https://pubs.rsc.org/en/content/articlelanding/2017/dt/c7dt01158j#!divAbstract
16. P. Rathi, M. K. Chahal and M. Sankar*, “Highly Electron Deficient Tetrabenzoquinone Appended Ni(II) and Cu(II) Porphyrins: Spectral, Solvatochromism, Electrochemical Redox and Tuneable F‒ and CN‒ Sensing Properties”, New J. Chem. 2017, 41, 11962-11968. https://pubs.rsc.org/en/content/articlelanding/2017/nj/c7nj01866e#!divAbstract
15. X. Ke, P. Yadav, L. Cong, R. Kumar, M. Sankar* and K. M. Kadish, “Facile and Reversible Electrogeneration of Porphyrin Trianions and Tetraanions in Nonaqueous Media from Electron Deficient β-Substituted Porphyrins”, Inorg. Chem. 2017, 56, 8527-8537. https://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.7b01262
14. P. Yadav, M. Sankar*, X. Ke, L. Cong and K. M. Kadish, “Synthesis of π-Extended Phenylethynyl Corroles and Their Intriguing Electrochemical Redox Properties”, Dalton Trans. 2017, 46, 10014-10022.
https://pubs.rsc.org/en/content/articlelanding/2017/dt/c7dt01814b#!divAbstract
13. P. Yadav, R. Kumar, A. Kumar and M. Sankar*, “β-Trisubstituted "Push-Pull" Porphyrins: Synthesis, Photophysical, Electrochemical and Theoretical Studies”, Eur. J. Inorg. Chem. 2017, 3269-3274.
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejic.201700310
12. M. K. Chahal, M. Sankar* and R. J. Butcher, “An Insight into Communication between β-olefin/phenyl olefin-mediated Acceptors and Porphyrin π-system: Way to establish Porphyrin based Chemodosimeters and Chemosensors”, Phys. Chem. Chem. Phys. 2017, 19, 4530-4540. https://pubs.rsc.org/en/content/articlelanding/2017/cp/c6cp08396j#!divAbstract
11. K. Prakash, S. Manchanda, V. Sudhakar, N. Sharma, M. Sankar* and K. Krishnamoorthy, “Facile Synthesis of β-Functionalized ‘Push-Pull’ Zn(II) Porphyrin for DSSC Applications”, Dyes Pigm. 2017, 147, 56-66. https://www.sciencedirect.com/science/article/abs/pii/S0143720817311099
10. P. Sonkar, K. Prakash, M. Yadav, V. Ganesan, M. Sankar*, R. Gupta and D. K. Yadav, “Co(II)-Porphyrins Decorated Carbon Nanotubes as Catalysts for Oxygen Reduction Reactions: An Approach for Fuel Cell Improvement”, J. Mater. Chem. A 2017, 5, 6263-6276.
https://pubs.rsc.org/en/content/articlelanding/2017/ta/c6ta10482g#!divAbstract
9. N. Grover, N. Chaudhri and M. Sankar*, “Facile Conversion of Ni(II) Cyclopropyl- chlorins into Novel β-Substituted Porphyrins through Acid-Catalyzed Ring-Opening Reaction”, Inorg. Chem. 2017, 56, 424-437. https://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.6b02333
8. K. Prakash and M. Sankar*, “Borylated Porphyrin and its Metal Complexes: Synthesis, Electrochemistry and Deprotection-Protection Strategy for Anion Sensing”, Sensor and Actuators: B Chemical 2017, 240, 709-717.
https://www.infona.pl/resource/bwmeta1.element.elsevier-ff33feb6-70f6-3286-abba-b2e646c6c77f
7. M. K. Chahal and M. Sankar*, “Switching between Porphyrin, Porphodimethene and Porphyrinogen using Cyanide and Fluoride ions mimicking Volatile Molecular Memory and 'NOR' Logic Gate”, Dalton Trans. 2016, 45, 16404-16412.
https://pubs.rsc.org/en/content/articlelanding/2016/dt/c6dt02506d#!divAbstract
6. N. Grover, M. Sankar*, Y. Song and K. M. Kadish, “Asymmetrically Crowded ‘Push-Pull’ Octaphenylporphyrins with Modulated Frontier Orbitals: Syntheses, Photophysical and Electrochemical Redox Properties”, Inorg. Chem. 2016, 55, 584-597 (Highlighted as HOT PAPER and one of the most read articles during Jan 2016). https://pubs.acs.org/doi/10.1021/acs.inorgchem.5b01339
5. R. Kumar, M. Sankar*, V. Sudhakar and K. Krishnamoorthy, “Synthesis and Characterisation of Simple Cost-effective Trans-A2BC-porphyrins with Various Donor Groups for Dye-Sensitized Solar Cells”, New. J. Chem. 2016, 40, 5704-5713 (an Invited article for the themed issue on Nitrogen Ligands). https://pubs.rsc.org/en/content/articlelanding/2016/nj/c5nj02610e#!divAbstract
4. R. Kumar, N. Chaudhary, M. Sankar* and M. R. Maurya, “Electron Deficient Nonplanar β-Octachlorovanadylporphyrin as Highly Efficient and Selective Epoxidation Catalyst for Olefins”, Dalton Trans. 2015, 44, 17720-17729.
https://pubs.rsc.org/en/content/articlelanding/2015/dt/c5dt02349a#!divAbstract
3. R. Kumar, N. Chaudhri, M. Sankar*, “Ratiometric and colorimetric “naked eye” selective detection of CN− ions by electron-deficient Ni(ii) porphyrins and their reversibility studies”, Dalton Trans. 2015, 44, 9149-9157 (One of the "Most accessed articles" during April 2015).
https://pubs.rsc.org/en/content/articlelanding/2015/dt/c5dt00937e#!divAbstract
2. R. Kumar, M. Sankar*, “Synthesis, Spectral, and Electrochemical Studies of Electronically Tunable β-Substituted Porphyrins with Mixed Substituent Pattern”, Inorg. Chem. 2014, 53, 12706-12719. https://pubs.acs.org/doi/10.1021/ic501259g
1. P. Yadav, M. Sankar*, “Synthesis, Spectroscopic and Electrochemical Studies of Phosphoryl and Carbomethoxy Substituted Corroles and their Anion Detection Properties”, Dalton Trans. 2014, 43, 14680-14688 (One of the "Most accessed articles" during August 2014).