1. M. Ottolini, Z. Anfar, N. Grover, G. Magna, M. Stefanelli, R. Paolesse, M. O. Senge, S. Bettini, L. Valli, R. Oda, G. Giancane 'Chirality induction to porphyrin derivatives co-confined at air-water interface with silica nano helices: towards enantioselective thin solid film surfaces.' Nanoscale. 2024, Accepted Article.

2. R. Kumar, N. Grover, N. Jain '1O2 Mediated Conversion of β-Enaminonitriles to α-Keto Amides Photosensitized by Recyclable H2TPP in Visible Light ' J. Org. Chem. 2024, 89, 4722-32.

3. K. Hemmer, S. M. Kronawitter, N. Grover, B. Twamley, M. Cokoja, R. A. Fischer, G. Kieslich, M. O. Senge 'Understanding and Controlling Molecular Compositions and Properties in Mixed-Linker Porphyrin Metal–Organic Frameworks.' Inorg. Chem. 2024, 63, 2122-30.

4. N. Grover, M. Cheveau, B. Twamley, C. J. Kingsbury, C. Mattern, and M. O. Senge 'Bicyclo [1.1.1] pentane embedded in porphyrinoids' Angew. Chem. Int. Ed., 2023, doi.org/10.1002/ange.202302771.

5. B.Yang, K. Niu, N. Cao, N. Grover, W. Zhao, A. Riss, J. Björk, W. Auwärter, J. V. Barth, and M. O. Senge 'On‐Surface synthesis of polyphenylene wires comprising rigid aliphatic bicyclo [1.1.1] pentane isolator units' Angew. Chem. Int. Ed., 2023, doi.org/10.1002/ange.202218211.

6. T. Ishizuka,^† N. Grover,^† C. J. Kingsbury, H. Kotani, M. O. Senge, and T. Kojima 'Nonplanar porphyrins: Synthesis, properties, and unique functionalities' Chem. Soc. Rev. 2022, 51, 7560–7630. ( ^†Authors contributed equally to work).

7. S. Shukla, N. Grover, P. Arora 'Resolution enhancement using a multi-layered Aluminum- based plasmonic device for chikungunya virus detection' Opt. Quantum Electron 2023, 55, 274.

8. R. Büchner, V. Vaz da Cruz, N. Grover, A. Charisiadis, M. Fondell, R. Haverkamp, M. O. Senge and A. Föhlisch 'Fundamental electronic changes upon intersystem crossing in large aromatic photosensitizers: free base 5, 10, 15, 20-tetrakis (4-carboxylatophenyl) porphyrin' Phys. Chem. Chem. Phys. 2022, 24, 7505–7511.

9. Y. M. Shaker, M. A. Omar, N. Grover, and M. O. Senge 'Facile synthesis of porphyrin-conjugates as amphiphilic modified photosensitizer structures of m-THPP bearing carbamate, carboxylate and sulfonate linkers' J. Porphyrins Phthalocyanines, 2022, 26, 630–647.

10. S. Bettini, N. Grover, M. Ottolini, C. Mattern, L. Valli, M. O. Senge, and G. Giancane 'Enantioselective discrimination of histidine by means of an achiral cubane-bridged bis-porphyrin' Langmuir 2021, 37, 13882–13889.

11. N. Grover, K. J. Flanagan, C. Trujillo, C. J. Kingsbury, and M. O. Senge 'An insight into non‐covalent interactions on the bicyclo [1.1. 1] pentane scaffold' Eur. J. Org. Chem. 2021, 1113-1122. (Selected for cover page illustration, Cover DOI: 10.1002/ejoc.202100101)

12. H. C. Sample, G. Emandi, B Twamley, N. Grover, B. Khurana, V. Sol, and M. O. Senge 'Synthesis and properties of BODIPY appended tetraphenylethylene scaffolds as photoactive arrays' Eur. J. Org. Chem. 2021, 4136-4143. (this work was also published in the noteworthy section of the Chemistry Views Magazine; Article Link: https://www.chemistryviews.org/details/ezine/11309382/BODIPY-Decorated_Tetraphenylethylenes.html)

13. N. Grover, G. M. Locke, K. J. Flanagan, M. H. R. Beh, A. Thompson, and M. O. Senge 'Bridging and conformational control of porphyrin units through non‐traditional rigid scaffolds' Chem. Eur. J. 2020, 26, 2405–2416. (HOT paper, Selected for cover page illustration, Cover DOI: 10.1002/chem.202000087).

14. N. Grover, and M. Sankar 'N‐Confused porphyrin – A unique “turn‐on” chemosensor for CN⁻ and F⁻ ions and “turn‐off” sensor for ClO₄⁻ ions' Chem. Asian J. 2020, 15, 2192–2197.

15. N. Grover, and M. O. Senge 'Synthetic advances in the C–H activation of rigid scaffold molecules' Synthesis 2020, 52, 3295–3325. (Invited Review, Most read article)

16. N. Grover, G. Emandi, B. Twamley, B. Khurana, V. Sol, and M. O. Senge 'Synthesis and structure of meso‐substituted dibenzihomoporphyrins' Eur. J. Org. Chem. 2020, 6489–6496. (VIP article; this work was also published in the noteworthy section of the Chemistry Views Magazine; Article Link: https://www.chemistryviews.org/details/ezine/11266523/New_Class_of_PorphyrinInspired_Macrocycles.html)

17. E. Sitte, B. Twamley, N. Grover, and M. O. Senge 'Investigation of the reactivity of 1-azido-3-iodobicyclo [1.1.1] pentane under “Click” reaction conditions' J. Org. Chem. 2021, 86, 1238–1245. (Selected for supplementary cover page illustration)

18. 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.

19. M. Kielmann, N. Grover, W. W. Kalisch, and M. O. Senge 'Incremental introduction of organocatalytic activity into conformationally engineered porphyrins' Eur. J. Org. Chem. 2019, 2448–2452. (Selected for cover page illustration, Cover DOI: 10.1002/ejoc.201900454)

20. N. Grover, N. Chaudhri, and M. Sankar 'β-Functionalized dibenzoporphyrins with mixed substituents pattern: facile synthesis, structural, spectral, and electrochemical redox properties' Inorg. Chem. 2019, 58, 2514–2522.

21. N. Grover, N. Chaudhri, and M. Sankar 'β-substituted donor-acceptor porphyrins: Synthesis, energy transfer and electrochemical redox properties' Dyes Pigm. 2019, 161, 104–112.

22. N. Chaudhri, L. Cong, N. Grover, W. Shan, K. Anshul, 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.

23. 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. (†These authors contributed equally)

24. N. Grover, R. Kumar, N. Chaudhri, R. Butcher, and M. Sankar 'β‐Heptasubstituted porphyrins: synthesis, structural, spectral, and electrochemical properties' Eur. J. Inorg. Chem. 2018, 3338–3343.

25. 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. (†These authors contributed equally)

26. 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, and electrochemical redox properties' Inorg. Chem. 2017, 56 11532–11545 (Highlighted as HOT PAPER on ACS website).

27. N. Grover,^† N. Chaudhri,^† and M. Sankar 'Facile conversion of Ni (II) cyclopropylchlorins into novel β-substituted porphyrins through acid-catalyzed ring-opening reaction' Inorg. Chem. 2017, 56, 424–437. (†These authors contributed equally)

28. 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 on ACS website and adjudged as one of the most accessed articles during Jan 2016).

29. N. Grover, P. Rathi, and M. Sankar 'Spectral investigations of meso-tetraalkylporphyrin-fullerene host–guest complexes' J. Porphyrins Phthalocyanines, 2015, 19, 997–1006. (Selected for cover page illustration).

30. N. Chaudhri,^† N. Grover,^† and M. Sankar 'Asymmetrically β-substituted porphyrins and chlorins: synthesis, spectroscopic, and electrochemical redox properties' ECS Transactions 2015, 66, 11–20. (†These authors contributed equally).