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Main-group Organometallic Functional Materials and Catalysis Lab (MOCL)
1. Swamy, P, C. A.* G. Sivaraman,* Priyanka R. N., Sufi O. R., Kandhasamy P., Jeyabalan S., Akash G.* Near Infrared (NIR) absorbing dyes as promising photosensitizer for photo dynamic therapy Coord. Chem. Rev., 2020, 411, 213233.https://doi.org/10.1016/j.ccr.2020.213233​
2. Swamy, P, C. A, Andrii Varenikov, and Graham de Ruiter* Direct Asymmetric Hydrogenation and Dynamic Kinetic Resolution of Aryl Ketones Catalyzed by an Iridium-NHC Exhibiting High Enantio- and Diastereoselectivity. Chem. Eur.J., 2020, 26, 2333 –2337.https://doi.org/10.1002/chem.201904911
3. Swamy, P, C. A., Andrii Varenikov, and Graham de Ruiter* Chiral Imidazo[1,5-a]pyridine–Oxazoline NHCs: A versatile Family of NHC ligands for the highly Enantioselective Hydrosilylation Ketones. Organometallics, 2020, 39, 247-257.https://doi.org/10.1021/acs.organomet.9b00526
4. Swamy, P, C. A.* Jeyabalan Shanmugapriya, Subramanian Singaravadivel, G. Sivaraman,* Duraisamy Chellappa “Anthracene-based highly Selective and Sensitive Fluorescent Turn-on Chemodosimeter for Hg2+. ACS Omega, 2018, 3, 12341–12348.https://doi.org/10.1021/acsomega.8b01142
5. Swamy, P, C. A.; Ephrath Solel; Ofer Reany;* Ehud Keinan* Synthetic Evolution of the Multifarene Cavity from Planar Predecessors. Chem. Eur. J., 2018, 24, 15319–15328.https://doi.org/10.1002/chem.201803189
6. Swamy, P, C. A.; Thilagar, P. Triarylborane-A2H2 and Triarylborane-Zn-A2H2 Porphyrin Conjugates: Synthesis, Structure and Intriguing Optical Properties. Dalton Trans., 2016, 45, 4688-4696.https://doi.org/10.1039/C5DT02678D
7. Swamy, P, C. A.; Thilagar, P. Polyfunctional Lewis acid: Intriguing Solid State Structure and Selective Detection and Discrimination of Nitroaromatic Explosives. Chem. Eur. J., 2015, 21, 8874 –8882.https://doi.org/10.1002/chem.201500727
8. Swamy, P, C. A.; Priyanka, R N.; Mukherjee, S.; Thilagar, P. Broadband Visible and NIR emissive, Panchromatic Borane-aza-BODIPY conjugate: Synthesis, Intriguing Optical Properties and Selective Fluorescent Sensing of Fluoride Anions. Eur. J. Inorg. Chem., 2015, 2338–2344.https://doi.org/10.1002/ejic.201500089
9. Swamy, P, C. A.; Mukherjee, S.; Thilagar, P. Dual Binding Site Assisted Chromogenic and Fluorogenic Recognition and Discrimination of Fluoride and Cyanide by a Peripherally BorylatedMetalloporphyrin: Overcoming Anion Interference in Organoboron Based Sensors. Anal. Chem., 2014, 86, 3616-3624.https://doi.org/10.1021/ac500230p
10. Swamy, P, C. A.; Thilagar, P. Triarylborane Appended New Triad and Tetrad: Chromogenic and Fluorogenic Anion Recognition. Inorg. Chem., 2014, 53, 2776–2786.https://doi.org/10.1021/ic402898n
11. Swamy, P, C. A.; Mukherjee, S.; Thilagar, P. Multichannel-Emissive V-shaped Boryl-BODIPY Dyads: Synthesis, Structure and Remarkably Diverse Response towards Fluoride. Inorg. Chem., 2014, 53, 4813–4823.https://doi.org/10.1021/ic402470a
12. Swamy, P, C. A.; Priyanka, R N.; Thilagar, P. Dual Receptor containing Triarylborane-Dipyrromethane conjugates: Synthesis and Evaluation of Anion Binding Site Preference fluoride ions. Dalton. Trans., 2014, 43, 4067-4075.https://doi.org/10.1039/C3DT52565A
13. Swamy, P, C. A.; Thilagar, P. Effect of substituent position on optical properties of Boron-Dipyrromethane isomers. Inorg. Chem. Acta., 2014, 411, 97-101.https://doi.org/10.1016/j.ica.2013.11.032
14. Swamy, P, C. A.; Mukherjee, S.; Thilagar, P. Dual emissive borane-BODIPY dyads: Molecular conformation control over electronic properties and fluorescence response towards fluoride ions. Chem. Commu., 2013, 49, 993-995.https://doi.org/10.1039/C2CC38352G
15. Swamy, P, C. A.; Mukherjee, S.; Thilagar, P. Tuning the solid state emission of meso-Me3SiC6H4 BODIPYs by tuning their solid state structure. J. Mater. Chem. C., 2013, 1, 4691- 4698.https://doi.org/10.1039/C3TC30632A
16. Thilagar, P.; Sudhakar, P.; Swamy, P, C. A.; Mukherjee, S. “Synthesis and spectral characterization of cyclotriphosphazene based 18-membered macrocycles”. Inorg. Chem. Acta., 2012, 390, 163-166.https://doi.org/10.1016/j.ica.2012.03.016
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