Publications

43. Biocidal polymer derived near white light-emitting carbonized polymeric dots for antibacterial and bioimaging applications. Sartaliya, S.; Sharma, R.; Sharma, A.; Chopra, V.; Ghosh, D.; Jayamurugan, G.* Photochem. Photobiol.  2024. Early view.  DOI: https://doi.org/10.1111/php.13912. Featured in the Front cover of the Journal (This article is part of a Special Issue dedicated to the topic of Photosciences in India)

2023

42. G. Jayamurugan,* S. Dhiman, S. Kumari, ORGANIC SMALL MOLECULE FLUORESCENT PROBE FOR DETECTING HYPO-AND HYPER-CHOLESTEROLEMIA. Indian Patent No. 202311086509

41. Efficient Nitric Oxide Scavenging by Urea-Functionalized Push-Pull Chromophore Modulates NO-Mediated Diseases. Roy, H. S.; Neethu, K. M.; Rajput, S.; Sadhukan,S.; Gowri, V.; Dar, A. H.; Monga, M.; Salaria,N.; Guha, R.; Chattopadhyayay, N.; Jayamurugan, G.* Ghosh, D.*  Chem. Eur. J.  2023.  DOI:10.1002/chem.202301748.

40. Perspectives on dual-purpose functional nanomaterials for detecting and removing fluoride ion from environmental water  Dhiman, S.; Solanki, A. K.; Nag, K.; Jayamurugan, G.* ChemNanoMat  2023.  DOI:10.1002/cnma.202300369. Featured in the Front cover of the Journal.

39. Superior Photophysical and Photosensitizing Properties of Nanoaggregates of Weekly Emissive Dye for Use in Bioimaging and Photodynamic Therapy.  Dar, A. H.; Ahmad, A.; Kumar, A.; Gowri, V.; Jori, C.; Sartaliya, S.; Neethu, K. M.; Khan, R.;* Jayamurugan, G.* Biomacromolecules  2023, 24, 5438-5450. DOI: https://doi.org/10.1021/acs.biomac.3c00892

38. A Study of [2+2] Cycloaddition–Retroelectrocyclization in Water: Observation of Substrate-driven Transient Nanoreactor Induced New Reactivity. Neethu,  k. M.; Kritika, N.; Dar, A. H.; Bajaj, A.; Gopal, S. A.; Gowri, V.; Mithilesh, N.; Sartaliya, S.; Sharma, R.; Solanki, A. K.; Ali, M. E.; Muthukrishnan, A.; Jayamurugan, G.* Org. Biomol. Chem.  2023, 21, 2922-2929.  DOI: https://doi.org/10.1039/D3OB00053B

2022

37. New Water-soluble Magnetic field-Induced Drug Delivery System Obtained Via Preferential Molecular Marriage over Narcissistic Self-Sorting. Sartaliya, S.; Mahajan, R.; Sharma, R.; Dar, A. H.;  Jayamurugan, G.* Langmuir  2022. 38, 8999-9009. (DOI: 10.1021/acs.langmuir.2c01403)

35. Cellulose-conjugated copper-oxide nanoparticles for the treatment of ethanol-induced gastric ulcer in wistar rats. Kumar, A.; Selim, A.; Gowri, V.; Ahmad, A.; Vyawahare, A.; Nadim, A.; Siddiqui, N.; Raza, S. S.; Jayamurugan, G.* R. Khan,* ACS Biomater. Sci. Eng. 2022, 8, 2636-2643. (DOI: 10.1021/acsbiomaterials.2c00090)

33. Thiol-Functionalized Cellulose-Grafted Copper Oxide Nanoparticles for the Therapy of Experimental Colitis in Swiss Albino Mice. Mishra, R. K.; Selim, A.; Gowri, V.; Ahmad, A.; Nadim, A.; Siddiqui, N.; Raza, S. S.; Jayamurugan, G.* R. Khan,* ACS Biomater. Sci. Eng. 2022, 8, 2088-2095. DOI: 10.1021/acsbiomaterials.2c00124. 

32. Unravelling the effect of non-drug spacers on a true drug-polymer and a comparative study of their antimicrobial activity. S. Sartaliya, V. Gowri, V. Chopra, H. S. Roy, D. Ghosh, G. Jayamurugan,* ACS Appl. Polym. Mater. 2022, 4, 3952-3961. (DOI: https://doi.org/10.1021/acsapm.2c00413).  Highlighted in the Front cover of the Journal.

31. Nanotechnology-assisted, single-chromophore-based white-light-emitting organic materials with bio-imaging properties. A. H. Dar, V. Gowri, R. K. Mishra, R. Khan, G. Jayamurugan,* Langmuir 2022, 38, 430–438. (DOI: 10.1021/acs.langmuir.1c02797). 

2021

30. Thiol-Functionalized Cellulose Wrapped Copperoxide as a Green Nano Catalyst for Regiospecific Azide–Alkyne Cycloaddition Reaction: Application in Rufinamide Synthesis. A. Selim, K. M. Neethu, V. Gowri, S. Sartaliya, S. Kaur, G. Jayamurugan,* Asian J. Org. Chem. 2021, 10, 3428-3433. (DOI: 10.1002/ajoc.202100658). 

29. A systematic study to unravel the potential of using polysaccharides based organic-nanoparticles versus hybrid-nanoparticles for pesticide delivery. R. Mahajan; A. Selim, K. M, Neethu, S. Sharma, V. Shanmugam, G. Jayamurugan,* Nanotechnology  2021, 32, 475704. (DOI: 10.1088/1361-6528/ac1bdc). 

28. A subtle change in substituent enabled multi-ways fluorine anion signals including paper-strip colorimetric detection using urea-functionalized push–pull chromophore receptor,  V. Gowri, S. Jalwal, A. H. Dar, A. Gopal, A. Muthukrishnan, A. Bajaj, M. E. Ali, G. Jayamurugan*, J. Photochem. Photobiol. A2021, 410, 113613 (DOI: 10.1016/j.jphotochem.2021.113163). 

27. M. M. Asari, A. Ahmad, A. Kumar, P. Alam, T. H. Khan, G. Jayamurugan, S. S. Raza, R. Khan,*  Aminocellulose-Grafted-Polycaprolactone Coated Gelatin Nanoparticles Alleviate Inflammation in Rheumatoid Arthritis: A Combinational Therapeutic ApproachCarbohydr. Polym. 2021, 117600.  (DOI: 10.1016/j.carbpol.2020.117600). 

2020

26. G. Jayamurugan,* V. Gowri, S. Jalwal, A. H. Dar, Non-planar push-pull chromophores for detection of fluoride (F) and method of preparing the same. Indian Patent No. 202011028595

25. Comparative acute intravenous toxicity study of triple polymer-layered magnetic nanoparticles with bare magnetic nanoparticles in Swiss albino mice,  A. Ahmad, M. M. Ansari, A. Kumar, A. Vyawahare, R. K. Mishra, G. Jayamurugan, S. S. Raza, R. Khan,* Nanotoxicology2020, 14, 1362-1380 (DOI: 10.1080/17435390.2020.1829144). 

22. Tuning of the Cross-Glaser Products mediated by Substrate-Catalyst’s Polymeric Backbone Interactions. S. Kaur, A. Mukhopadhyaya, A. Selim, V. Gowri, K. M. Neethu, A. H. Dar, S. Sartaliya,  M. E. Ali* and G. Jayamurugan*, Chem. Commun., 2020, 56, 2582-2585. DOI:10.1039/C9CC08565C

20. A. Ahmad, A. Gupta, M. M. Ansari, A. Vyawahare, G. Jayamurugan,* R. Khan,* Hyperbranched polymer-functionalized magnetic nanoparticles mediatd hyperthermia and niclosamide bimodal therapy of Colorectal Cance Cells, ACS Biomater. Sci. Eng. 2020, 6, 1102-1111. DOI:10.1021/acsbiomaterials.9b01947

2019

19. G. Jayamurugan,* A. Selim, S. Kaur, K. M. Neethu, V. Gowri, M. E. Ali, Thiol functionalized polymers bearing catalytic nanoparticles method of preparing the same and use thereof, Patent no. 201911042361.

18. Designing of Push–Pull Chromophores with Tunable Electronic and Luminescent Properties Using Urea as the Electron DonorA. H. Dar, V. Gowri, A. Gopal, A. Muthukrishnan, A. Bajaj, S. Sartaliya, A. Selim, Md. E. Ali, G. Jayamurugan*  J. Org. Chem.  2019, 84, 8941-8947.  DOI: doi.org/10.1021/acs.joc.9b00841

2006-2016

16.  G. Jayamurugan, V. Gowri, D. Hernández, S. Martin, A. González-Orive, C. Dengiz, O. Dumele, F. Pérez-Murano, J.-P. Gisselbrecht, C. Boudon, W. B. Schweizer, B. Breiten, A. D. Finke, G. Jeschke, B. Bernet, L. Ruhlmann, P. Cea, F. Diederich, “Design and Synthesis of Aviram–Ratner-Type Dyads and Rectification Studies in Langmuir–Blodgett (LB) Films”, Chem. Eur. J. 2016, 22, 10539−10547. (selected as Hot paper

15. M. L. Böhm, T. C. Jellicoe, J. P. H. Rivett, A. Sadhanala, N. J. L. K. Davis, F. S. F. Morgenstern, K. C. Gödel, G. Jayamurugan, C. G. M. Benson, N. C. Greenham, B. Ehrler, “Size and Energy Level Tuning of Quantum Dot Solids via a Hybrid Ligand Complex” J. Phys. Chem. Lett. 2015, 6, 3510−3514.

14. G. Jayamurugan, D. A. Roberts, T. K. Ronson, J. R. Nitschke, “Selective endo and exo binding of mono- and ditopic-ligands to a rhomboidal diporphyrin prism”, Angew. Chem. Int. Ed. 2015, 54, 7539−7543. 

13. G. Jayamurugan, A. D. Finke, J.-P. Gisselbrecht, C. Boudon, W. B. Schweizer, F. Diederich, “One-Pot access to push-pull oligoenes by sequential [2+2] cycloaddition–retroelectrocyclization reactions,” J. Org. Chem. 2014, 79, 426–431.

12. P. T. Ullas, S. N. Madhusudana, A. Desai, G. Jayamurugan, N. Jayaraman, “Enhancement of immunogenicity and efficacy of a plasmid DNA rabies vaccine by nanoformulation with a fourth-generation amine-terminated poly(ether imine) dendrimer,” Int. J. Nanomedicine 2014, 9, 627–634. 

11. G. Jayamurugan, O. Dumele, J.-P. Gisselbrecht, C. Boudon, W. B. Schweizer, B. Bernet, F. Diederich, “Expanding the chemical structure space of optoelectronic molecular materials: unprecedented push–pull chromophores by reaction of a donor-substituted tetracyanofulvene with electron-rich alkynes”, J. Am. Chem. Soc. 2013, 135, 3599–3606.

10. R. S. Bagul, Y. B. R. D. Rajesh, G. Jayamurugan, A. Bera, A. K. Sood, N. Jayaraman, “Photophysical behavior of poly(propyl ether imine) dendrimer in the presence of nitroaromatic compounds”, J. Photochem. Photobiol., A 2013, 253, 1–6.

9. A. D. Finke, O. Dumele, M. Zalibera, D. Confortin, P. Cias, G. Jayamurugan, J.-P. Gisselbrecht, C. Boudon, W. B. Schweizer, G. Gescheidt, F. Diederich, “6,6-Dicyanopentafulvenes: Electronic structure and regioselectivity in [2 + 2] cycloaddition–retroelectrocyclization reactions”, J. Am. Chem. Soc. 2012, 134, 18139–18146.

8. G. Jayamurugan, J.-P. Gisselbrecht, C. Boudon, F. Schoenebeck, W. B. Schweizer, B. Bernet, F. Diederich, “Expanding the chemical space for push-pull chromophores by non-concerted [2+2] and [4+2] cycloadditions: access to a highly functionalized 6,6-dicyanofulvene with an intense low-energy charge–transfer band”, Chem. Commun. 2011, 47, 4520–4522.

7. G. Jayamurugan, K. S. Vasu, Y. B. R. D. Rajesh, S. Kumar, V. Vasumathi, P. K. Maiti, A. K. Sood, N. Jayaraman, “Interaction of single-walled carbon nanotubes with poly(propyl ether imine) dendrimers”, J. Chem. Phys. 2011, 134, 104507/1–104507/6.

6. U. P. Thankappan, S. N. Madhusudana, A. Desai, G. Jayamurugan, Y. B. R. D. Rajesh, N. Jayaraman, “Dendritic poly(ether imine) based gene delivery vector”, Bioconjugate Chem. 2011, 22, 115–119.

5. G. Jayamurugan, N. Jayaraman, “Increased efficacies of an individual catalytic site in clustered multivalent dendritic catalysts”, Adv. Synth. Catal. 2009, 351, 2379–2390.

4. G. Jayamurugan, C. P. Umesh, N. Jayaraman, “Preparation and catalytic studies of palladium nanoparticles stabilized by a dendritic ligand-functionalized Silica”, JMol. Catal. A: Chem. 2009, 307, 142–148.

3. G. Jayamurugan, C. P. Umesh, N. Jayaraman, “Inherent photoluminescence properties of poly(propyl ether imine) dendrimers”, Org. Lett. 2008, 10, 9–12.

2. C. Jana, G. Jayamurugan, R. Ganapathy, P. K. Maiti, N. Jayaraman, A. K. Sood, “Structure of poly(propyl ether imine) dendrimer from fully atomistic molecular dynamics simulation and by small angle X-ray scattering”, J. Chem. Phys. 2006, 124, 204719/1–204719/10.

1. G. Jayamurugan, N. Jayaraman, “Synthesis of large generation poly(propyl ether imine) (PETIM) dendrimers”, Tetrahedron 2006, 62, 9582–9588.

     Patents 

4. G. Jayamurugan,* A. Selim, S. Kaur, K. M. Neethu, V. Gowri, M. E. Ali, Thiol functionalized polymers bearing catalytic nanoparticles method of preparing the same and use thereof, Patent filing no. 201911042361, 2019. 

3. N. Jayaraman, G. Jayamurugan, Y. B. R. D. Rajesh, R. Bhaskara, B. Suresh, A. K. Sood, “A method for detecting an analyte”, PCT Int. Appl. WO 2011030313, 2011, 18 pp.; US patent App, US 20120171776, 2011.

2.  N. Jayaraman, P. U. Thankappan, N. S. Madhusudana, A. Desai, G. Jayamurugan, Yamajala B. R. D. Rajesh, “New poly(ether imine) dendrimers useful in preparing polymer system for deleivering negatively charged moleucle e.g. nucliec acid, DNA, polynucleotides, short interfering RNA, micro RNA and ribozymes, into cells”, PCT Int. Appl. WO 2012090223-A1, 2012.

1.  G. Jayamurugan, N. Jayaraman, “Poly(ether imine) dendrimers and uses thereof”, Indian pat. Appl. IN2010CH04010, 2014, 64 pp. 

     Book Chapters

Conferences

1.   A. D. Finke, O. Dumele, G. Jayamurugan, J.-P. Gisselbrecht, C. Boudon, W. B. Schweizer, F. Diederich, F. “Fulvenoid, nonplanar push-pull chromophores.” Poster presentation at the Electronic Process in Organic Materials Gordon Conference, Lucca, Italy, June 3-8, 2012.

2.   G. Jayamurugan, F. Schoenebeck, W. B. Schweizer, B. Bernet, J.-P. Gisselbrecht, C. Boudon, F. Diederich, “Wisenshaftforumchemie”  September 4-7, 2011, Bremen / Germany _ Poster: “Expanding the Chemical Space for Push-Pull chromophores by Non-concerted [2+2] and [4+2] Cycloadditions: Access to a Highly Functionalized 6,6-dicyanopentafulvene with Attractive Opto-electronic Properties”.

3.   G. Jayamurugan, O. Dumele, W. B. Schweizer, B. Bernet, J.-P. Gisselbrecht, C. Boudon, F. Diederich, “Swiss Chemical Society” August 29 - September 2, 2011, ETH-Zurich / Switzerland _ Poster: “Diverse Chemical Reactivity of Push-Pull type Fulvene with Electron Rich Alkynes”.

4.   G. Jayamurugan, B. B. Frank, M. Kivala, W. B. Schweizer, B. C. Blanco, B. Breiten, R. R. Tykwinski, E. Jahnke, C. Boudon, J.-P. Gisselbrecht, F. Diederich, “3rd EuCheMS Chemistry Congress” August 29 - September 2, 2010, Nürnberg / Germany _ Poster: “Synthesis and Studies of Chiral and Achiral Push-Pull Type Charge-Transfer Chromophores Derived from Different Oligoyne”.

5.   G. Jayamurugan, N. Jayaraman, “Synthesis and Studies of Poly(Propyl Ether Imine) (PETIM) Dendrimers.” 10th Chemical Research Society of India, National Symposium (CRSI symposium), February 2008, Indian Institute of Science, Bangalore, India.

6.   G. Jayamurugan, N. Jayaraman, “Synthesis and Studies of Poly(Ether Imine) (PETIM) Dendritic Macromolecules”. National Conference on Chemistry, September 2006, Bangalore University, Bangalore, India.

7.   G. Jayamurugan, N. Jayaraman, “International Symposium in Organic Chemistry” 23rd December 2005, IISc, Bangalore, India _ Poster Presentation: “Synthesis and Fluorescence Studies of Poly(Propyl Ether Imine) (PETIM) Dendrimers”.