Jing Li, Hongjiang Ren, Jiangtao Li, Liuchang Wang
{"title":"两种新型配位聚合物:晶体结构和荧光特性。","authors":"Jing Li, Hongjiang Ren, Jiangtao Li, Liuchang Wang","doi":"10.1007/s10895-024-04025-9","DOIUrl":null,"url":null,"abstract":"<p><p>A new Ni (II) metal-organic frameworks with the formula [Ni<sub>2</sub>(HL)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>]∙3H<sub>2</sub>O (1) and a novel phenoxo-O bridged rare-earth dinuclear Schiff base complex with the formula [La<sub>2</sub>(dbm)<sub>4</sub>L·CH<sub>3</sub>OH] (2), where the HL<sup>2-</sup> is the partial deprotonated of the organic ligand H<sub>3</sub>L, and H<sub>2</sub>L is a bis-Schiff foundation ligand (H<sub>3</sub>L = 4,6-dioxo-1,4,5,6-tetrahydro-1,3,5-triazine-2-carboxylic acid, H<sub>2</sub>L = N, N'-bis (2-hydroxy-3-methoxybenzylidene) -propane-1,2-diamine, Hdbm = dibenzoylmethane), have been successfully generated under the solvothermal condition. The targeted product sample of 1 and 2 has been fully characterized by single-crystal X-ray data, elemental analysis, FT-IR, powder X-ray diffraction, and thermogravimetric analysis. Furthermore, fluorescence performance testing of the complexes revealed that in complex 1, H<sub>3</sub>L forms a rigid chain through coordination with Ni<sup>2+</sup> ions and further forms a highly rigid three-dimensional framework within the hydrogen bond network, resulting in fluorescence enhancement of up to 13.7-fold, displaying deep blue fluorescence with CIE coordinates of (0.1626, 0.1375). In contrast, complex 2 forms only discrete zero-dimensional molecules and exhibits light blue fluorescence with CIE coordinates of (0.1744, 0.2306). This demonstrates their potential as fluorescent materials.</p>","PeriodicalId":15800,"journal":{"name":"Journal of Fluorescence","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Two New Coordination Polymers: Crystal Structures and Fluorescence Properties.\",\"authors\":\"Jing Li, Hongjiang Ren, Jiangtao Li, Liuchang Wang\",\"doi\":\"10.1007/s10895-024-04025-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A new Ni (II) metal-organic frameworks with the formula [Ni<sub>2</sub>(HL)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>]∙3H<sub>2</sub>O (1) and a novel phenoxo-O bridged rare-earth dinuclear Schiff base complex with the formula [La<sub>2</sub>(dbm)<sub>4</sub>L·CH<sub>3</sub>OH] (2), where the HL<sup>2-</sup> is the partial deprotonated of the organic ligand H<sub>3</sub>L, and H<sub>2</sub>L is a bis-Schiff foundation ligand (H<sub>3</sub>L = 4,6-dioxo-1,4,5,6-tetrahydro-1,3,5-triazine-2-carboxylic acid, H<sub>2</sub>L = N, N'-bis (2-hydroxy-3-methoxybenzylidene) -propane-1,2-diamine, Hdbm = dibenzoylmethane), have been successfully generated under the solvothermal condition. The targeted product sample of 1 and 2 has been fully characterized by single-crystal X-ray data, elemental analysis, FT-IR, powder X-ray diffraction, and thermogravimetric analysis. Furthermore, fluorescence performance testing of the complexes revealed that in complex 1, H<sub>3</sub>L forms a rigid chain through coordination with Ni<sup>2+</sup> ions and further forms a highly rigid three-dimensional framework within the hydrogen bond network, resulting in fluorescence enhancement of up to 13.7-fold, displaying deep blue fluorescence with CIE coordinates of (0.1626, 0.1375). In contrast, complex 2 forms only discrete zero-dimensional molecules and exhibits light blue fluorescence with CIE coordinates of (0.1744, 0.2306). This demonstrates their potential as fluorescent materials.</p>\",\"PeriodicalId\":15800,\"journal\":{\"name\":\"Journal of Fluorescence\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-11-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Fluorescence\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1007/s10895-024-04025-9\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fluorescence","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s10895-024-04025-9","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
Two New Coordination Polymers: Crystal Structures and Fluorescence Properties.
A new Ni (II) metal-organic frameworks with the formula [Ni2(HL)2(H2O)4]∙3H2O (1) and a novel phenoxo-O bridged rare-earth dinuclear Schiff base complex with the formula [La2(dbm)4L·CH3OH] (2), where the HL2- is the partial deprotonated of the organic ligand H3L, and H2L is a bis-Schiff foundation ligand (H3L = 4,6-dioxo-1,4,5,6-tetrahydro-1,3,5-triazine-2-carboxylic acid, H2L = N, N'-bis (2-hydroxy-3-methoxybenzylidene) -propane-1,2-diamine, Hdbm = dibenzoylmethane), have been successfully generated under the solvothermal condition. The targeted product sample of 1 and 2 has been fully characterized by single-crystal X-ray data, elemental analysis, FT-IR, powder X-ray diffraction, and thermogravimetric analysis. Furthermore, fluorescence performance testing of the complexes revealed that in complex 1, H3L forms a rigid chain through coordination with Ni2+ ions and further forms a highly rigid three-dimensional framework within the hydrogen bond network, resulting in fluorescence enhancement of up to 13.7-fold, displaying deep blue fluorescence with CIE coordinates of (0.1626, 0.1375). In contrast, complex 2 forms only discrete zero-dimensional molecules and exhibits light blue fluorescence with CIE coordinates of (0.1744, 0.2306). This demonstrates their potential as fluorescent materials.
期刊介绍:
Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.