journal article·2026

Engineering the amorphous-to-crystalline transformation, fluorescence enhancement and reversible switching of a cyclobutane derivative inside a polymer film

Supriya Kar, Sonu Kumari, Ram Singh Jat, Ch. Suresh, S. Rajagopala Reddy, M. Bhanuchandra, Chanchayya Gupta Chandaluri

Journal of Materials Chemistry C· Volume 14· Issue 27
Publisher page

Abstract

A polymer matrix approach enables reversible amorphous-to-crystalline transformation and fluorescence switching of CB in a polymer thin film. Computational modelling provided insights into the mechanism enhancing solid-state fluorescence emission.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Supramolecular Chemistry and Complexes · Surface Chemistry and Catalysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Humanities and Sciences, Chemistry Division, Indian Institute of Petroleum and Energy, Visakhapatnam, Andhra Pradesh-530003, India

Department of Chemistry, Central University of Rajasthan, Bandarsindri, Rajasthan-305817, India

Department of Chemistry, University of Delhi, Delhi-110007, India

Funding

Science and Engineering Research Board

References (56)

Show source-provided references
1. Li · Aggregate · 2021 · 2 · e5110.1002/agt2.51 ↗
2. Chua · Mater. Chem. Front. · 2021 · 5 · 65910.1039/D0QM00607F ↗
3. Liu · Aggregate · 2021 · 2 · e3410.1002/agt2.34 ↗
4. Zhan · Adv. Mater. Technol. · 2025 · 10 · e0136610.1002/admt.202501366 ↗
5. Hou · Nat. Commun. · 2015 · 6 · 688410.1038/ncomms7884 ↗
6. Hwang · Aggregate · 2023 · 4 · e19910.1002/agt2.199 ↗
7. Wang · Acc. Mater. Res. · 2023 · 4 · 31110.1021/accountsmr.2c00158 ↗
8. Maurya · Adv. Opt. Mater. · 2024 · 12 · 230227910.1002/adom.202302279 ↗
9. Hong · Chem. Soc. Rev. · 2011 · 40 · 536110.1039/c1cs15113d ↗
10. Suzuki · Angew. Chem. · 2020 · 132 · 994010.1002/ange.202000940 ↗
11. Chen · Chem. Mater. · 2003 · 15 · 153510.1021/cm021715z ↗
12. Dong · Chem. Commun. · 2007 · 325510.1039/b704794k ↗
13. Zhang · J. Mater. Chem. C · 2014 · 2 · 508310.1039/C4TC00221K ↗
14. Chandaluri · J. Mater. Chem. C · 2013 · 1 · 446410.1039/c3tc30615a ↗
15. Mali · Cryst. Growth Des. · 2022 · 22 · 189210.1021/acs.cgd.1c01459 ↗
16. Z.Yang , Z.Chi , Z.Mao , Y.Zhang , S.Liu , J.Zhao , M. P.Aldred and Z.Chi , Materials Chemistry Frontiers , Royal Society of Chemistry , 2018 , vol. 2, pp. 861–890
17. Li · Chem. Soc. Rev. · 2020 · 49 · 151710.1039/C9CS00098D ↗
18. Hariharan · J. Mater. Chem. C · 2015 · 3 · 838110.1039/C5TC01369K ↗
19. Srujana · Chem. – Eur. J. · 2018 · 24 · 178410.1002/chem.201705041 ↗
20. Wang · Mater. Horizons · 2021 · 8 · 63010.1039/D0MH01251C ↗
21. Zhang · J. Lumin. · 2022 · 241 · 11852510.1016/j.jlumin.2021.118525 ↗
22. Dou · J. Phys. Chem. Lett. · 2011 · 2 · 66610.1021/jz200140c ↗
23. Zhao · Mater. Chem. Front. · 2018 · 2 · 159510.1039/C8QM00130H ↗
24. Arockiam · Sens. Actuators, B · 2017 · 242 · 53510.1016/j.snb.2016.11.086 ↗
25. Srujana · Angew. Chem. · 2015 · 127 · 737810.1002/ange.201501032 ↗
26. Sudhakar · Chem. – Asian J. · 2019 · 14 · 475410.1002/asia.201901086 ↗
27. Wang · Angew. Chem., Int. Ed. · 2020 · 59 · 1758010.1002/anie.202005933 ↗
28. Liu · Angew. Chem., Int. Ed. · 2020 · 59 · 1509810.1002/anie.202002220 ↗
29. Chandaluri · Angew. Chem., Int. Ed. · 2012 · 51 · 1184910.1002/anie.201205081 ↗
30. Ito · Sci. Rep. · 2016 · 6 · 2291810.1038/srep22918 ↗
31. Ito · ChemPhysChem · 2021 · 22 · 166210.1002/cphc.202100370 ↗
32. Bronshtein · Small · 2019 · 15 · 190293610.1002/smll.201902936 ↗
33. Jat · Asian J. Org. Chem. · 2025 · 14 · e20250037410.1002/ajoc.202500374 ↗
34. Zandler · C. R. Chim. · 2006 · 9 · 96010.1016/j.crci.2005.12.008 ↗
35. Orio · Photosynth. Res. · 2009 · 102 · 44310.1007/s11120-009-9404-8 ↗
36. Chen · Front. Phys. China · 2006 · 1 · 33910.1007/s11467-006-0026-8 ↗
37. Wang · J. Comput. Chem. · 2020 · 41 · 171810.1002/jcc.26213 ↗
38. Tegegn · Sci. Rep. · 2024 · 14 · 814610.1038/s41598-024-58599-2 ↗
39. El Mouhi · Res. Chem. Intermed. · 2019 · 45 · 132710.1007/s11164-018-3674-8 ↗
40. Jendoubi · J. Comput. Chem. · 2024 · 45 · 56310.1002/jcc.27270 ↗
41. El-Demerdash · Sci. Rep. · 2023 · 13 · 1562610.1038/s41598-023-42450-1 ↗
42. Tirado-Rives · J. Chem. Theory Comput. · 2008 · 4 · 29710.1021/ct700248k ↗
43. M.Aydin , Density Functional Theory-Recent Advances, New Perspectives and Applications , InTech , Rijeka , 2019
44. D’Cunha · J. Phys. Chem. A · 2021 · 125 · 309510.1021/acs.jpca.1c00803 ↗
45. Hernández-Lima · Front. Chem. · 2022 · 10 · 101276910.3389/fchem.2022.1012769 ↗
46. Machado · J. Phys. Chem. C · 2016 · 120 · 1766010.1021/acs.jpcc.6b01567 ↗
47. Marenich · J. Phys. Chem. B · 2009 · 113 · 637810.1021/jp810292n ↗
48. Takano · J. Chem. Theory Comput. · 2005 · 1 · 7010.1021/ct049977a ↗
49. L.Xu , Towards Improving The Accuracy of Implicit Solvent Models and Understanding Electrostatic Catalysis in Complex Solvent Environment , The Australian National University , 2022
50. Neese · J. Chem. Phys. · 2020 · 152 · 22410810.1063/5.0004608 ↗
51. Neese · Faraday Discuss. · 2024 · 254 · 29510.1039/D4FD00056K ↗
52. Neese · Wiley Interdiscip. Rev.: Comput. Mol. Sci. · 2012 · 2 · 73
53. Guareschi · J. Chem. Theory Comput. · 2013 · 9 · 551310.1021/ct400876y ↗
54. Plasser · J. Chem. Phys. · 2020 · 152 · 08410810.1063/1.5143076 ↗
55. J. R.Lakowicz , Principles of fluorescence spectroscopy , 200610.1007/978-0-387-46312-4 ↗
56. CCDC 2488778: Experimental Crystal Structure Determination , 2026 10.5517/ccdc.csd.cc2pjs5610.5517/ccdc.csd.cc2pjs56 ↗