Fang-Wen Lv, Xue-Ting Wang, Cheng Chen, Jun Zheng and Xiu-Ying Zheng*,
{"title":"圆偏振发光手性双核镧系团簇的结构-旋热性质研究","authors":"Fang-Wen Lv, Xue-Ting Wang, Cheng Chen, Jun Zheng and Xiu-Ying Zheng*, ","doi":"10.1021/acs.cgd.5c0047010.1021/acs.cgd.5c00470","DOIUrl":null,"url":null,"abstract":"<p >The luminescence quantum yield (Φ<sub>lum</sub>) and dissymmetry factor (<i>g</i><sub>lum</sub>) are two critical parameters for evaluating the performance of circularly polarized luminescence (CPL) materials. In this work, three pairs of chiral lanthanide clusters <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-pH</b>, <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-BH</b>, and <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b> exhibiting CPL properties were synthesized using <i>R</i>-/<i>S</i>-HL (<i>R</i>-HL = <i>R</i>-(−)-2-phenylpropionic acid, <i>S</i>-HL = <i>S</i>-(+)-2-phenylpropionic acid) as the chiral ligand. Intermolecular interactions within these compounds were fine-tuned by varying the types and coordination numbers of auxiliary ligands (phen = 1,10-phenanthroline, Hfac = hexafluoroacetylacetone, and Bphen = bathophenanthroline). As a result, the three pairs of compounds exhibited slightly different Φ<sub>lum</sub> values ((93.7 ± 0.8)% for <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-pH</b>, (83.8 ± 0.8)% for <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-BH</b>, and (87.5 ± 0.7)% for <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b>). These variations are attributed to the difference in intermolecular interactions with both π–π and H−π stacking observed in <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-pH</b>, weak π–π stacking in <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-BH</b>, and moderate H−π stacking in <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b>. Additionally, <i>g</i><sub>lum</sub> can be effectively controlled by modulating the chiral environment and the symmetry of the geometric coordination configuration of the Ln<sup>3+</sup> ions. Among the three pairs of compounds, <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b> displayed the largest <i>g</i><sub>lum</sub> values (−0.025/0.022), owing to the presence of more chiral ligands coordinated and a lower symmetry in the Eu<sup>3+</sup> coordination environment, compared to <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-pH</b> (−0.0042/0.0043) and <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-BH</b> (−0.0058/0.0042). Consequently, <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b> achieves improvement of <i>g</i><sub>lum</sub> while maintaining a high Φ<sub>lum</sub> value. Additionally, <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b> showed excellent detection capability of DCN in pesticide optical recognition, with a detection limit as low as 0.37 μM. This study not only elucidates the regulatory effects of intermolecular interactions and chiral environments on the CPL performance of chiral lanthanide clusters but also provides new insights into their potential application in environmental detection.</p>","PeriodicalId":34,"journal":{"name":"Crystal Growth & Design","volume":"25 11","pages":"4026–4034 4026–4034"},"PeriodicalIF":3.2000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Insights into the Structure–Chiroptical Property in Families of Chiral Binuclear Lanthanide Clusters with Circularly Polarized Luminescence\",\"authors\":\"Fang-Wen Lv, Xue-Ting Wang, Cheng Chen, Jun Zheng and Xiu-Ying Zheng*, \",\"doi\":\"10.1021/acs.cgd.5c0047010.1021/acs.cgd.5c00470\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The luminescence quantum yield (Φ<sub>lum</sub>) and dissymmetry factor (<i>g</i><sub>lum</sub>) are two critical parameters for evaluating the performance of circularly polarized luminescence (CPL) materials. In this work, three pairs of chiral lanthanide clusters <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-pH</b>, <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-BH</b>, and <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b> exhibiting CPL properties were synthesized using <i>R</i>-/<i>S</i>-HL (<i>R</i>-HL = <i>R</i>-(−)-2-phenylpropionic acid, <i>S</i>-HL = <i>S</i>-(+)-2-phenylpropionic acid) as the chiral ligand. Intermolecular interactions within these compounds were fine-tuned by varying the types and coordination numbers of auxiliary ligands (phen = 1,10-phenanthroline, Hfac = hexafluoroacetylacetone, and Bphen = bathophenanthroline). As a result, the three pairs of compounds exhibited slightly different Φ<sub>lum</sub> values ((93.7 ± 0.8)% for <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-pH</b>, (83.8 ± 0.8)% for <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-BH</b>, and (87.5 ± 0.7)% for <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b>). These variations are attributed to the difference in intermolecular interactions with both π–π and H−π stacking observed in <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-pH</b>, weak π–π stacking in <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-BH</b>, and moderate H−π stacking in <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b>. Additionally, <i>g</i><sub>lum</sub> can be effectively controlled by modulating the chiral environment and the symmetry of the geometric coordination configuration of the Ln<sup>3+</sup> ions. Among the three pairs of compounds, <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b> displayed the largest <i>g</i><sub>lum</sub> values (−0.025/0.022), owing to the presence of more chiral ligands coordinated and a lower symmetry in the Eu<sup>3+</sup> coordination environment, compared to <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-pH</b> (−0.0042/0.0043) and <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-BH</b> (−0.0058/0.0042). Consequently, <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b> achieves improvement of <i>g</i><sub>lum</sub> while maintaining a high Φ<sub>lum</sub> value. Additionally, <b><i>R</i>-/<i>S</i>-Eu</b><sub><b>2</b></sub><b>-B</b> showed excellent detection capability of DCN in pesticide optical recognition, with a detection limit as low as 0.37 μM. This study not only elucidates the regulatory effects of intermolecular interactions and chiral environments on the CPL performance of chiral lanthanide clusters but also provides new insights into their potential application in environmental detection.</p>\",\"PeriodicalId\":34,\"journal\":{\"name\":\"Crystal Growth & Design\",\"volume\":\"25 11\",\"pages\":\"4026–4034 4026–4034\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Crystal Growth & Design\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.cgd.5c00470\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Crystal Growth & Design","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.cgd.5c00470","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Insights into the Structure–Chiroptical Property in Families of Chiral Binuclear Lanthanide Clusters with Circularly Polarized Luminescence
The luminescence quantum yield (Φlum) and dissymmetry factor (glum) are two critical parameters for evaluating the performance of circularly polarized luminescence (CPL) materials. In this work, three pairs of chiral lanthanide clusters R-/S-Eu2-pH, R-/S-Eu2-BH, and R-/S-Eu2-B exhibiting CPL properties were synthesized using R-/S-HL (R-HL = R-(−)-2-phenylpropionic acid, S-HL = S-(+)-2-phenylpropionic acid) as the chiral ligand. Intermolecular interactions within these compounds were fine-tuned by varying the types and coordination numbers of auxiliary ligands (phen = 1,10-phenanthroline, Hfac = hexafluoroacetylacetone, and Bphen = bathophenanthroline). As a result, the three pairs of compounds exhibited slightly different Φlum values ((93.7 ± 0.8)% for R-/S-Eu2-pH, (83.8 ± 0.8)% for R-/S-Eu2-BH, and (87.5 ± 0.7)% for R-/S-Eu2-B). These variations are attributed to the difference in intermolecular interactions with both π–π and H−π stacking observed in R-/S-Eu2-pH, weak π–π stacking in R-/S-Eu2-BH, and moderate H−π stacking in R-/S-Eu2-B. Additionally, glum can be effectively controlled by modulating the chiral environment and the symmetry of the geometric coordination configuration of the Ln3+ ions. Among the three pairs of compounds, R-/S-Eu2-B displayed the largest glum values (−0.025/0.022), owing to the presence of more chiral ligands coordinated and a lower symmetry in the Eu3+ coordination environment, compared to R-/S-Eu2-pH (−0.0042/0.0043) and R-/S-Eu2-BH (−0.0058/0.0042). Consequently, R-/S-Eu2-B achieves improvement of glum while maintaining a high Φlum value. Additionally, R-/S-Eu2-B showed excellent detection capability of DCN in pesticide optical recognition, with a detection limit as low as 0.37 μM. This study not only elucidates the regulatory effects of intermolecular interactions and chiral environments on the CPL performance of chiral lanthanide clusters but also provides new insights into their potential application in environmental detection.
期刊介绍:
The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials.
Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.