Green regioselective synthesis and theoretical insights into photo- and thermochromic spiro heterocycles: toward optical and thermal sensing applications
Abstract Building on the significant potential of pyrimidine-based molecules for optoelectronic applications, we designed and synthesized a new series of spiro[indoline-pyrido-pyrimidine] derivatives with excellent selectivity. These compounds exhibit novel photochromic and thermochromic properties,...
| Published in: | Scientific Reports |
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| Main Authors: | , , , , , |
| Format: | Article |
| Language: | English |
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Nature Portfolio
2025-07-01
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| Online Access: | https://doi.org/10.1038/s41598-025-03431-8 |
| _version_ | 1849500345610272768 |
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| author | Marzieh Jamali Ali R. Sardarian Farideh Rezaei Afshan Mohajeri Mohammad M. Ghanbari Gyula Batta |
| author_facet | Marzieh Jamali Ali R. Sardarian Farideh Rezaei Afshan Mohajeri Mohammad M. Ghanbari Gyula Batta |
| author_sort | Marzieh Jamali |
| collection | DOAJ |
| container_title | Scientific Reports |
| description | Abstract Building on the significant potential of pyrimidine-based molecules for optoelectronic applications, we designed and synthesized a new series of spiro[indoline-pyrido-pyrimidine] derivatives with excellent selectivity. These compounds exhibit novel photochromic and thermochromic properties, addressing the growing need for diagnostic agents with minimal side effects. The regioisomers were identified using 1D, 2D homonuclear and heteronuclear correlation NMR spectroscopy, along with X-ray crystallography. Dynamic 1 H NMR (DNMR) studies revealed that the major isomer (4 sa) is more stable than the minor isomer (4 sb). Optical, electrochemical, and structural analyses of compounds 4aa, 4ab, 4 sa, and 4sb demonstrated the feasibility of chemical reactions converting closed-ring structures to open-ring structures, resulting in notable optical properties due to ring opening. To validate the experimental data, density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations were conducted at the B3LYP/6-31G(d) level, offering insights into the electronic structure and absorption spectra. Additionally, Gibbs free energy (ΔG) calculations were performed to elucidate the proposed mechanism for open-ring compounds named 5 and 7. This work emphasizes employing the citric acid as a bio-organic catalyst in a green, multi-component domino reaction, underscoring its environmentally sustainable approach. These studies reveal the potential of these compounds for advanced optical and temperature sensing applications, aligning theoretical and experimental approaches to establish a robust foundation for future research. |
| format | Article |
| id | doaj-art-e93e9e5fe13a4be08bc3caad58acab68 |
| institution | Directory of Open Access Journals |
| issn | 2045-2322 |
| language | English |
| publishDate | 2025-07-01 |
| publisher | Nature Portfolio |
| record_format | Article |
| spelling | doaj-art-e93e9e5fe13a4be08bc3caad58acab682025-08-20T03:03:36ZengNature PortfolioScientific Reports2045-23222025-07-0115112010.1038/s41598-025-03431-8Green regioselective synthesis and theoretical insights into photo- and thermochromic spiro heterocycles: toward optical and thermal sensing applicationsMarzieh Jamali0Ali R. Sardarian1Farideh Rezaei2Afshan Mohajeri3Mohammad M. Ghanbari4Gyula Batta5Chemistry Department, College of Science, Shiraz UniversityChemistry Department, College of Science, Shiraz UniversityChemistry Department, College of Science, Shiraz UniversityChemistry Department, College of Science, Shiraz UniversityChemistry Department, Sarvestan Branch, Islamic Azad UniversityOrganic Chemistry Department, University of DebrecenAbstract Building on the significant potential of pyrimidine-based molecules for optoelectronic applications, we designed and synthesized a new series of spiro[indoline-pyrido-pyrimidine] derivatives with excellent selectivity. These compounds exhibit novel photochromic and thermochromic properties, addressing the growing need for diagnostic agents with minimal side effects. The regioisomers were identified using 1D, 2D homonuclear and heteronuclear correlation NMR spectroscopy, along with X-ray crystallography. Dynamic 1 H NMR (DNMR) studies revealed that the major isomer (4 sa) is more stable than the minor isomer (4 sb). Optical, electrochemical, and structural analyses of compounds 4aa, 4ab, 4 sa, and 4sb demonstrated the feasibility of chemical reactions converting closed-ring structures to open-ring structures, resulting in notable optical properties due to ring opening. To validate the experimental data, density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations were conducted at the B3LYP/6-31G(d) level, offering insights into the electronic structure and absorption spectra. Additionally, Gibbs free energy (ΔG) calculations were performed to elucidate the proposed mechanism for open-ring compounds named 5 and 7. This work emphasizes employing the citric acid as a bio-organic catalyst in a green, multi-component domino reaction, underscoring its environmentally sustainable approach. These studies reveal the potential of these compounds for advanced optical and temperature sensing applications, aligning theoretical and experimental approaches to establish a robust foundation for future research.https://doi.org/10.1038/s41598-025-03431-8Spiro[indoline-pyrido-pyrimidine]Regioselective synthesisPhoto and thermochromic compoundGreen multicomponent reactionNatural catalystDensity functional theory |
| spellingShingle | Marzieh Jamali Ali R. Sardarian Farideh Rezaei Afshan Mohajeri Mohammad M. Ghanbari Gyula Batta Green regioselective synthesis and theoretical insights into photo- and thermochromic spiro heterocycles: toward optical and thermal sensing applications Spiro[indoline-pyrido-pyrimidine] Regioselective synthesis Photo and thermochromic compound Green multicomponent reaction Natural catalyst Density functional theory |
| title | Green regioselective synthesis and theoretical insights into photo- and thermochromic spiro heterocycles: toward optical and thermal sensing applications |
| title_full | Green regioselective synthesis and theoretical insights into photo- and thermochromic spiro heterocycles: toward optical and thermal sensing applications |
| title_fullStr | Green regioselective synthesis and theoretical insights into photo- and thermochromic spiro heterocycles: toward optical and thermal sensing applications |
| title_full_unstemmed | Green regioselective synthesis and theoretical insights into photo- and thermochromic spiro heterocycles: toward optical and thermal sensing applications |
| title_short | Green regioselective synthesis and theoretical insights into photo- and thermochromic spiro heterocycles: toward optical and thermal sensing applications |
| title_sort | green regioselective synthesis and theoretical insights into photo and thermochromic spiro heterocycles toward optical and thermal sensing applications |
| topic | Spiro[indoline-pyrido-pyrimidine] Regioselective synthesis Photo and thermochromic compound Green multicomponent reaction Natural catalyst Density functional theory |
| url | https://doi.org/10.1038/s41598-025-03431-8 |
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