CN106192011A - 一种二阶非线性光学晶体材料的制备方法 - Google Patents
一种二阶非线性光学晶体材料的制备方法 Download PDFInfo
- Publication number
- CN106192011A CN106192011A CN201610807281.0A CN201610807281A CN106192011A CN 106192011 A CN106192011 A CN 106192011A CN 201610807281 A CN201610807281 A CN 201610807281A CN 106192011 A CN106192011 A CN 106192011A
- Authority
- CN
- China
- Prior art keywords
- nonlinear optical
- order nonlinear
- metal
- organic framework
- preparation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 230000003287 optical effect Effects 0.000 title claims abstract description 20
- 239000013078 crystal Substances 0.000 title claims abstract description 14
- 239000000463 material Substances 0.000 title claims abstract description 13
- 238000002360 preparation method Methods 0.000 title claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 241000080590 Niso Species 0.000 claims abstract description 9
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 9
- 239000011734 sodium Substances 0.000 claims abstract description 9
- MWVTWFVJZLCBMC-UHFFFAOYSA-N 4,4'-bipyridine Chemical compound C1=NC=CC(C=2C=CN=CC=2)=C1 MWVTWFVJZLCBMC-UHFFFAOYSA-N 0.000 claims abstract description 8
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 abstract description 12
- 239000012621 metal-organic framework Substances 0.000 abstract description 12
- 239000003446 ligand Substances 0.000 abstract description 9
- 230000005291 magnetic effect Effects 0.000 abstract description 7
- 229910021645 metal ion Inorganic materials 0.000 abstract description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 abstract description 4
- 230000005290 antiferromagnetic effect Effects 0.000 abstract description 3
- 230000008878 coupling Effects 0.000 abstract description 3
- 238000010168 coupling process Methods 0.000 abstract description 3
- 238000005859 coupling reaction Methods 0.000 abstract description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract description 2
- 239000004202 carbamide Substances 0.000 abstract description 2
- 238000010586 diagram Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- WBPWDGRYHFQTRC-UHFFFAOYSA-N 2-ethoxycyclohexan-1-one Chemical compound CCOC1CCCCC1=O WBPWDGRYHFQTRC-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000002189 fluorescence spectrum Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- GQYHUHYESMUTHG-UHFFFAOYSA-N lithium niobate Chemical compound [Li+].[O-][Nb](=O)=O GQYHUHYESMUTHG-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/46—Sulfur-, selenium- or tellurium-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B7/00—Single-crystal growth from solutions using solvents which are liquid at normal temperature, e.g. aqueous solutions
- C30B7/14—Single-crystal growth from solutions using solvents which are liquid at normal temperature, e.g. aqueous solutions the crystallising materials being formed by chemical reactions in the solution
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Pyridine Compounds (AREA)
Abstract
本发明涉及一种二阶非线性光学晶体材料的制备方法,其包括下述步骤:将NiSO4·6H2O、4,4’‑联吡啶、间苯二甲酸‑5‑磺酸钠溶于水中;搅拌2 h,然后,封装在25 mL的反应釜中,120 °C加热36 h;冷却到室温有蓝色晶体生成。本发明中的金属有机框架化合物不同于其他二阶非线性光学金属有机框架化合物,其利用对称结构的配体与金属离子合成得到的一种具有非心结构的金属有机框架化合物。其二阶非线性光学性质是尿素的0.8倍,还具有相位匹配。同时还具有荧光发射性质以及磁学性质。其荧光发射峰在416 nm,与配体相比,发生了红移。在28 K时孤对电子转变成反铁磁耦合。
Description
技术领域
本发明涉及一种二阶非线性光学材料,尤其涉及一种二阶非线性光学晶体材料的制备方法。
背景技术
现有的二阶非线性光学材料多集中在碘酸锂、铌酸锂等以及半导体晶体,如碲和淡红银矿(Ag3AsS3)等。因为这些二阶非线性材料的热稳定性良好,在较高温度时不发生分解。所以迅速成为研究的热点,该类报道比较多见。但现有的二阶非线性光学性质的金属有机框架化合物多以不对称的配体为原料,与金属离子构成非心结构,二阶非线性光学性质不够理想,而且不具有荧光性质以及磁学性质。
发明内容
本发明针对上述现有技术中存在的问题,提供了一种二阶非线性光学晶体材料的制备方法,不仅提高了二阶非线性光学性质,还具有荧光性质以及磁学性质。
本发明的技术方案如下:
将1-1.5mmol 的NiSO4·6H2O、1-1.5mmol 的4,4’-联吡啶、1-1.5mmol的间苯二甲酸-5-磺酸钠溶于水中;搅拌2 h,然后,封装在25 mL的反应釜中,120 °C加热36 h;冷却到室温有蓝色晶体生成,产率约为75-84%。
所述的NiSO4·6H2O与水质量体积比为,0.263-0.395 gNiSO4·6H2O溶于20 mL水中。
本发明与其它二阶非线性光学材料相比,金属有机框架化合物材料具有以下几个突出的特点:(1)具有良好的热稳定性;(2)配体的结构、官能团以及共轭程度均可事先设计;(3)拓展二阶非线性光学材料的种类,将其拓展到金属有机框架化合物,并且利用对称结构的配体与金属离子进行合成;(4)将合成二阶非线性材料具有可以设计性,不但具有二阶非线性光学性质,还具有荧光性质以及磁学性质。
本发明是利用对称结构的两种配体间苯二甲酸-5-磺酸钠以及4,4’-联吡啶与过渡金属离子配位形成的金属有机框架化合物。本发明中的金属有机框架化合物不同于其他二阶非线性光学金属有机框架化合物,其利用对称结构的配体与金属离子合成得到的一种具有非心结构的金属有机框架化合物。其二阶非线性光学性质是尿素的0.8倍,还具有相位匹配。同时还具有荧光发射性质以及磁学性质。其荧光发射峰在416 nm,与配体相比,发生了红移。在28 K时孤对电子转变成反铁磁耦合。
附图说明
图1为金属有机框架化合物的分子结构示意图。
图2为热重曲线示意图。
图3为荧光发射光谱示意图。
图4为二阶非线性光学性质示意图。
图5a在1000 Oe磁场条件下,χM -1-T图。
图5b在1000 Oe磁场条件下,χM-T和χMT-T图。
其中,图3中L为 间苯二甲酸-5-磺酸钠,1为金属有机框架化合物。
具体实施方式
实施例1
将0.263 g NiSO4·6H2O ( 1mmol)、0.156 g 4,4’-联吡啶( 1mmol)、0.268 g间苯二甲酸-5-磺酸钠(1mmol)溶于20mL水中,搅拌2 h,然后,封装在25mL的反应釜中,120 °C加热36 h,冷却到室温有蓝色晶体生成,产率约为75%。
结论:由附图1得知,配合物1为新颖的配合物;由附图2得知,配合物1在200 ℃条件下只失去水分子,整体结构没有塌陷;由附图3得知,配合物1的荧光发射峰相对于配体发生红移;由附图4得知,配合物1具有二阶非线性光学性质;由附图5得知,配合物1具有反铁磁耦合。
实施例2
将0.395g的NiSO4·6H2O、0.234g4,4’-联吡啶、0.402g间苯二甲酸-5-磺酸钠溶于20mL水中。搅拌2 h,然后,封装在25mL的反应釜中,120 °C加热36 h。冷却到室温有蓝色晶体生成,产率约为75-84%。
实施例3
将0.329gNiSO4·6H2O、0.195g的4,4’-联吡啶、0.335g间苯二甲酸-5-磺酸钠溶于20mL水中。搅拌2 h,然后,封装在25 mL的反应釜中,120 °C加热36 h。冷却到室温有蓝色晶体生成,产率约为75-84%。
实施例4
将0.263gNiSO4·6H2O、0.234g 4,4’-联吡啶、0.268g间苯二甲酸-5-磺酸钠溶于20 mL水中。搅拌2 h,然后,封装在25mL的反应釜中,120 °C加热36 h。冷却到室温有蓝色晶体生成,产率约为75-84%。
Claims (2)
1.一种二阶非线性光学晶体材料的制备方法,其特征在于包括下述步骤:将1-1.5mmol的NiSO4·6H2O、1-1.5mmol 的4,4’-联吡啶、1-1.5mmol的间苯二甲酸-5-磺酸钠溶于水中;搅拌2 h,然后,封装在25mL的反应釜中,120 °C加热36 h;冷却到室温有蓝色晶体生成。
2.根据权利要求1所述的一种二阶非线性光学晶体材料的制备方法,其特征在于所述的NiSO4·6H2O与水质量体积比为,0.263-0.395 gNiSO4·6H2O溶于20mL水中。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610807281.0A CN106192011B (zh) | 2016-09-07 | 2016-09-07 | 一种二阶非线性光学晶体材料的制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610807281.0A CN106192011B (zh) | 2016-09-07 | 2016-09-07 | 一种二阶非线性光学晶体材料的制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106192011A true CN106192011A (zh) | 2016-12-07 |
CN106192011B CN106192011B (zh) | 2018-10-02 |
Family
ID=58068242
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610807281.0A Active CN106192011B (zh) | 2016-09-07 | 2016-09-07 | 一种二阶非线性光学晶体材料的制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106192011B (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112961532A (zh) * | 2021-02-08 | 2021-06-15 | 米格(浙江)创新科技有限公司 | 超宽波幅红外线保温隔热涂料 |
CN115611801A (zh) * | 2022-09-16 | 2023-01-17 | 中南大学 | 一种二阶非线性光学材料及其制备方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103951709A (zh) * | 2014-04-25 | 2014-07-30 | 衡阳师范学院 | 一种茂基过渡金属镍氮配合物及其制备方法和应用 |
CN104098613A (zh) * | 2014-07-14 | 2014-10-15 | 天津师范大学 | 混合配体Dy(III)-Ni(II)混金属磁性配合物及其制备方法与应用 |
KR20150136459A (ko) * | 2015-11-16 | 2015-12-07 | 국립대학법인 울산과학기술대학교 산학협력단 | 단일 결정성 중공 금속-유기 골격체의 제조 방법 |
CN105237576A (zh) * | 2015-10-19 | 2016-01-13 | 桂林理工大学 | 三核锰配合物及其制备方法 |
KR101625487B1 (ko) * | 2014-04-10 | 2016-05-30 | 울산과학기술원 | 단일 결정성 중공 금속-유기 골격체의 제조 방법 |
-
2016
- 2016-09-07 CN CN201610807281.0A patent/CN106192011B/zh active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101625487B1 (ko) * | 2014-04-10 | 2016-05-30 | 울산과학기술원 | 단일 결정성 중공 금속-유기 골격체의 제조 방법 |
CN103951709A (zh) * | 2014-04-25 | 2014-07-30 | 衡阳师范学院 | 一种茂基过渡金属镍氮配合物及其制备方法和应用 |
CN104098613A (zh) * | 2014-07-14 | 2014-10-15 | 天津师范大学 | 混合配体Dy(III)-Ni(II)混金属磁性配合物及其制备方法与应用 |
CN105237576A (zh) * | 2015-10-19 | 2016-01-13 | 桂林理工大学 | 三核锰配合物及其制备方法 |
KR20150136459A (ko) * | 2015-11-16 | 2015-12-07 | 국립대학법인 울산과학기술대학교 산학협력단 | 단일 결정성 중공 금속-유기 골격체의 제조 방법 |
Non-Patent Citations (6)
Title |
---|
《化工百科全书》编辑委员会: "《化工百科全书 第8卷 计算机控制系统—聚硅氧烷 ji-ju》", 31 December 1994 * |
BING-YU ZHANG,ET AL.: "Poly[octa-l-aqua-tetraaquabis(l4-5-sulfonatobenzene-1,3-dicarboxylato)-nickel(II)tetrasodium]", 《ACTA CRYSTALLOGRAPHICA SECTION E》 * |
DAOFENG SUN,ET AL.: "Syntheses and structures of two novel copper complexes constructed from unusual planar tetracopper(II) SBUs", 《CHEM. COMMUN.》 * |
HONG-XU GUO,ET AL.: "Synthesis and characterizations of a novel 2-D organic–inorganic hybrid constructed from mixed ligands and mixed-valence copper(I/II)", 《INORGANIC CHEMISTRY COMMUNICATIONS》 * |
XING LI, ET AL.: "Self-Assembly of 1D to 3D Cadmium Complexes: Structural Characterization and Properties", 《EUR. J. INORG. CHEM.》 * |
YU-LING WANG,ET AL.: "Two novel luminescent silver(I) coordination polymers containing octanuclear silver cluster units or ligand unsupported Ag/Ag interactions constructed from 5-sulfoisophthalic acid (H3SIP) and organic amine", 《CRYSTENGCOMM》 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112961532A (zh) * | 2021-02-08 | 2021-06-15 | 米格(浙江)创新科技有限公司 | 超宽波幅红外线保温隔热涂料 |
CN112961532B (zh) * | 2021-02-08 | 2022-07-05 | 米格(浙江)创新科技有限公司 | 超宽波幅红外线保温隔热涂料 |
CN115611801A (zh) * | 2022-09-16 | 2023-01-17 | 中南大学 | 一种二阶非线性光学材料及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN106192011B (zh) | 2018-10-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Liu et al. | Silver (I) coordination polymers of fluorescent oligo (phenylenevinylene) with π− π Stackings: luminescence and conductivity | |
CN108949148B (zh) | 一种稀土超分子凝胶荧光材料及其制备方法 | |
Fang et al. | Designing organic room temperature phosphorescence with ultralong lifetime by substituent modification | |
CN106565781A (zh) | 含有膦的二苯酮类有机发光材料及其合成方法与应用 | |
Guan et al. | Tricolor Luminescence Switching by Thermal and Mechanical Stimuli in the Crystal Polymorphs of Pyridyl‐substituted Fluorene | |
Ji et al. | Synthesis, Structure, and Photoluminescence of Color-Tunable and White-Light-Emitting Lanthanide Metal–Organic Open Frameworks Composed of AlMo6 (OH) 6O183–Polyanion and Nicotinate | |
CN106192011B (zh) | 一种二阶非线性光学晶体材料的制备方法 | |
CN107089944A (zh) | 基于2‑甲基‑5,7‑二氯‑8‑羟基喹啉为配体的单核镝配合物及其制备方法和应用 | |
CN108165261A (zh) | 一种基于三联吡啶配体的多色发光凝胶及其制备方法与应用 | |
Xie et al. | Long-persistent high-temperature phosphorescence of zero-dimensional metal halide hybrid for temperature-sensitive anticounterfeiting | |
Chi et al. | Pt (II) Complexes with Azolate‐containing Bidentate Chelate: Design, Photophysics, and Application | |
CN107445902A (zh) | 一种苯并咪唑硫酸盐的制备、结构及荧光性质 | |
Jin et al. | Synthesis and Structural Characterization of Four Zinc Complexes Containing 3, 5‐Dimethylpyrazole and Carboxylate Ligands | |
CN108997389B (zh) | 8-羟基喹啉衍生物和1,10-邻菲啰啉混合掺杂的镝配合物及其制备方法和应用 | |
CN103554083A (zh) | 一种具有蓝光性能镉配位化合物的单晶结构和制备方法 | |
CN103224783B (zh) | 一种具有紫光性能4-[(8-羟基-5-喹啉)偶氮]苯磺酸镉配合物的制备方法 | |
CN107936948A (zh) | 一种具有荧光性质的金属铽配位聚合物及其制备方法 | |
Wu et al. | UV-Curing Resin-Assisted Facile Synthesis of Lead-Free Zero-Dimensional Organic–Inorganic Hybrid Metal Halide Quantum Dots for Light-Emitting Application | |
CN112979527B (zh) | 具有长波长室温磷光发射的卤代酰亚胺材料和应用 | |
CN106478468A (zh) | 一种基于π‑π堆积化合物的荧光材料及其制备方法 | |
CN103665007B (zh) | 1,1-二(1-h-苯并咪唑基)甲烷-银(i)配合物及制备方法 | |
CN114751838A (zh) | 4,4′,4″-三甲酸三苯胺的绿色合成工艺 | |
CN107118240B (zh) | 一种提高铕的配合物发光效率的方法 | |
CN106544011B (zh) | 一种具有抗磁性链状配位聚合物的制备方法 | |
Gao et al. | Organic Ligand Exchange: The Chiral Structure–Property Regulation of Cuprous Halides |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |