两种新型配位聚合物:晶体结构和荧光特性。

IF 2.6 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
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}
引用次数: 0

摘要

一种新的镍(II)金属有机框架,其化学式为[Ni2(HL)2(H2O)4]∙3H2O (1),以及一种新的苯氧-O 桥接稀土二核席夫基地复合物,其化学式为[La2(dbm)4L-CH3OH](2),其中 HL2- 是有机配体 H3L 的部分去质子化、H3L=4,6-二氧代-1,4,5,6-四氢-1,3,5-三嗪-2-羧酸,H2L=N,N'-双(2-羟基-3-甲氧基亚苄基)-1,2-丙二胺,Hdbm=二苯甲酰甲烷)。通过单晶 X 射线数据、元素分析、傅立叶变换红外光谱、粉末 X 射线衍射和热重分析,对 1 和 2 的目标产品样品进行了全面表征。此外,对复合物进行的荧光性能测试表明,在复合物 1 中,H3L 通过与 Ni2+ 离子配位形成一条刚性链,并在氢键网络中进一步形成一个高度刚性的三维框架,从而使荧光增强高达 13.7 倍,显示出 CIE 坐标为(0.1626, 0.1375)的深蓝色荧光。相比之下,复合物 2 只形成离散的零维分子,并显示出淡蓝色荧光,CIE 坐标为(0.1744, 0.2306)。这表明它们具有作为荧光材料的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信