Abbas Khaja Raees Ahmed, Ramalingam Gajendhiran, Sivaraj Mithra, Seepoo Abdul Majeed, Azeez Sait Sahul Hameed, Rajakkani Paulpandiyan, Subbaiah Maniyammai, Gurusamy Thangavelu Senthil Andavan, MohamedHanifa NizamMohideen, Aziz Kalilur Rahiman
{"title":"用于选择性检测 Zn2+、Al3+ 和 F- 离子的基于水杨醛的双响应 \"开启 \"荧光化学传感器:理论研究以及在斑马鱼幼体活细胞成像和分子逻辑门操作中的应用。","authors":"Abbas Khaja Raees Ahmed, Ramalingam Gajendhiran, Sivaraj Mithra, Seepoo Abdul Majeed, Azeez Sait Sahul Hameed, Rajakkani Paulpandiyan, Subbaiah Maniyammai, Gurusamy Thangavelu Senthil Andavan, MohamedHanifa NizamMohideen, Aziz Kalilur Rahiman","doi":"10.1039/d4tb01356e","DOIUrl":null,"url":null,"abstract":"<p><p>Four salicylidene-based dual-responsive chemosensors 1,5-bis(5-bromosalicylaldehyde)carbohydrazone (R1), 1,5-bis(5-bromosalicylaldehyde)thiocarbohydrazone (R2), 1,5-bis(3-ethoxysalicylaldehyde)carbohydrazone (R3) and 1,5-bis(3-ethoxysalicylaldehyde)thiocarbohydrazone (R4) were synthesized and characterized. The molecular structures of R1 and R3 were confirmed by single crystal X-ray diffraction technique, which crystallized in the orthorhombic <i>Pbcn</i> and monoclinic <i>P</i>2<sub>1</sub>/<i>n</i> space groups, respectively. The chemosensor molecules were investigated for their recognition properties against the selected cations (K<sup>+</sup>, Ca<sup>2+</sup>, Mn<sup>2+</sup>, Co<sup>2+</sup>, Ni<sup>2+</sup>, Cu<sup>2+</sup>, Zn<sup>2+</sup>, Fe<sup>3+</sup> and Al<sup>3+</sup>) and anions (F<sup>-</sup>, Cl<sup>-</sup>, Br<sup>-</sup>, I<sup>-</sup>, HSO<sub>4</sub><sup>-</sup>, H<sub>2</sub>PO<sub>4</sub><sup>-</sup>, ClO<sub>4</sub><sup>-</sup>, N<sub>3</sub><sup>-</sup> and NO<sub>3</sub><sup>-</sup>) by colorimetry, absorption spectroscopy, fluorescence spectroscopy, <sup>1</sup>H NMR spectroscopy and theoretical studies. The sensor molecules showed colorimetric responses for the Co<sup>2+</sup>, Ni<sup>2+</sup>, Cu<sup>2+</sup> and Fe<sup>3+</sup> cations and the F<sup>-</sup> anion. Interestingly, the Zn<sup>2+</sup> and Al<sup>3+</sup> cations showed only the 'turn on' fluorometric response, whereas the F<sup>-</sup> anion showed both colorimetric and fluorometric responses. The binding constants were determined using the Benesi-Hildebrand (B-H) equation from the fluorescence titrations and found to be higher for R3 towards the Al<sup>3+</sup> cation (2.03 × 10<sup>6</sup> M<sup>-1</sup>) with a low limit of detection (1.79 μM) and for R4 towards the F<sup>-</sup> anion (5.13 × 10<sup>5</sup> M<sup>-1</sup>) with a low limit of detection (5.23 μM). The chemosensors established 1 : 2 and 1 : 1 binding stoichiometries with the sensed cations and anion, respectively, as confirmed by Job's plots. The computational studies show a lower band gap of HOMO-LUMO when the chemosensors bind with the sensed inorganic ions compared to the free chemosensors. Furthermore, the observed fluorescent behaviour of the Zn<sup>2+</sup> and Al<sup>3+</sup> cations have motivated us to investigate the practical applications in the live cell-imaging of zebrafish larvae as well as in the development of a molecular logic gate.</p>","PeriodicalId":94089,"journal":{"name":"Journal of materials chemistry. B","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Salicylidene-based dual-responsive 'turn on' fluorometric chemosensors for the selective detection of Zn<sup>2+</sup>, Al<sup>3+</sup> and F<sup>-</sup> ions: theoretical investigation and applications in the live cell imaging of zebrafish larvae and molecular logic gate operation.\",\"authors\":\"Abbas Khaja Raees Ahmed, Ramalingam Gajendhiran, Sivaraj Mithra, Seepoo Abdul Majeed, Azeez Sait Sahul Hameed, Rajakkani Paulpandiyan, Subbaiah Maniyammai, Gurusamy Thangavelu Senthil Andavan, MohamedHanifa NizamMohideen, Aziz Kalilur Rahiman\",\"doi\":\"10.1039/d4tb01356e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Four salicylidene-based dual-responsive chemosensors 1,5-bis(5-bromosalicylaldehyde)carbohydrazone (R1), 1,5-bis(5-bromosalicylaldehyde)thiocarbohydrazone (R2), 1,5-bis(3-ethoxysalicylaldehyde)carbohydrazone (R3) and 1,5-bis(3-ethoxysalicylaldehyde)thiocarbohydrazone (R4) were synthesized and characterized. The molecular structures of R1 and R3 were confirmed by single crystal X-ray diffraction technique, which crystallized in the orthorhombic <i>Pbcn</i> and monoclinic <i>P</i>2<sub>1</sub>/<i>n</i> space groups, respectively. The chemosensor molecules were investigated for their recognition properties against the selected cations (K<sup>+</sup>, Ca<sup>2+</sup>, Mn<sup>2+</sup>, Co<sup>2+</sup>, Ni<sup>2+</sup>, Cu<sup>2+</sup>, Zn<sup>2+</sup>, Fe<sup>3+</sup> and Al<sup>3+</sup>) and anions (F<sup>-</sup>, Cl<sup>-</sup>, Br<sup>-</sup>, I<sup>-</sup>, HSO<sub>4</sub><sup>-</sup>, H<sub>2</sub>PO<sub>4</sub><sup>-</sup>, ClO<sub>4</sub><sup>-</sup>, N<sub>3</sub><sup>-</sup> and NO<sub>3</sub><sup>-</sup>) by colorimetry, absorption spectroscopy, fluorescence spectroscopy, <sup>1</sup>H NMR spectroscopy and theoretical studies. The sensor molecules showed colorimetric responses for the Co<sup>2+</sup>, Ni<sup>2+</sup>, Cu<sup>2+</sup> and Fe<sup>3+</sup> cations and the F<sup>-</sup> anion. Interestingly, the Zn<sup>2+</sup> and Al<sup>3+</sup> cations showed only the 'turn on' fluorometric response, whereas the F<sup>-</sup> anion showed both colorimetric and fluorometric responses. The binding constants were determined using the Benesi-Hildebrand (B-H) equation from the fluorescence titrations and found to be higher for R3 towards the Al<sup>3+</sup> cation (2.03 × 10<sup>6</sup> M<sup>-1</sup>) with a low limit of detection (1.79 μM) and for R4 towards the F<sup>-</sup> anion (5.13 × 10<sup>5</sup> M<sup>-1</sup>) with a low limit of detection (5.23 μM). The chemosensors established 1 : 2 and 1 : 1 binding stoichiometries with the sensed cations and anion, respectively, as confirmed by Job's plots. The computational studies show a lower band gap of HOMO-LUMO when the chemosensors bind with the sensed inorganic ions compared to the free chemosensors. Furthermore, the observed fluorescent behaviour of the Zn<sup>2+</sup> and Al<sup>3+</sup> cations have motivated us to investigate the practical applications in the live cell-imaging of zebrafish larvae as well as in the development of a molecular logic gate.</p>\",\"PeriodicalId\":94089,\"journal\":{\"name\":\"Journal of materials chemistry. B\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-11-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of materials chemistry. B\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/d4tb01356e\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of materials chemistry. B","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/d4tb01356e","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Salicylidene-based dual-responsive 'turn on' fluorometric chemosensors for the selective detection of Zn2+, Al3+ and F- ions: theoretical investigation and applications in the live cell imaging of zebrafish larvae and molecular logic gate operation.
Four salicylidene-based dual-responsive chemosensors 1,5-bis(5-bromosalicylaldehyde)carbohydrazone (R1), 1,5-bis(5-bromosalicylaldehyde)thiocarbohydrazone (R2), 1,5-bis(3-ethoxysalicylaldehyde)carbohydrazone (R3) and 1,5-bis(3-ethoxysalicylaldehyde)thiocarbohydrazone (R4) were synthesized and characterized. The molecular structures of R1 and R3 were confirmed by single crystal X-ray diffraction technique, which crystallized in the orthorhombic Pbcn and monoclinic P21/n space groups, respectively. The chemosensor molecules were investigated for their recognition properties against the selected cations (K+, Ca2+, Mn2+, Co2+, Ni2+, Cu2+, Zn2+, Fe3+ and Al3+) and anions (F-, Cl-, Br-, I-, HSO4-, H2PO4-, ClO4-, N3- and NO3-) by colorimetry, absorption spectroscopy, fluorescence spectroscopy, 1H NMR spectroscopy and theoretical studies. The sensor molecules showed colorimetric responses for the Co2+, Ni2+, Cu2+ and Fe3+ cations and the F- anion. Interestingly, the Zn2+ and Al3+ cations showed only the 'turn on' fluorometric response, whereas the F- anion showed both colorimetric and fluorometric responses. The binding constants were determined using the Benesi-Hildebrand (B-H) equation from the fluorescence titrations and found to be higher for R3 towards the Al3+ cation (2.03 × 106 M-1) with a low limit of detection (1.79 μM) and for R4 towards the F- anion (5.13 × 105 M-1) with a low limit of detection (5.23 μM). The chemosensors established 1 : 2 and 1 : 1 binding stoichiometries with the sensed cations and anion, respectively, as confirmed by Job's plots. The computational studies show a lower band gap of HOMO-LUMO when the chemosensors bind with the sensed inorganic ions compared to the free chemosensors. Furthermore, the observed fluorescent behaviour of the Zn2+ and Al3+ cations have motivated us to investigate the practical applications in the live cell-imaging of zebrafish larvae as well as in the development of a molecular logic gate.