CN105694862A - Luminescent material [Zn(tibc)2]n and synthetic method - Google Patents
Luminescent material [Zn(tibc)2]n and synthetic method Download PDFInfo
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- CN105694862A CN105694862A CN201610171237.5A CN201610171237A CN105694862A CN 105694862 A CN105694862 A CN 105694862A CN 201610171237 A CN201610171237 A CN 201610171237A CN 105694862 A CN105694862 A CN 105694862A
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- 239000000463 material Substances 0.000 title claims abstract description 10
- 238000010189 synthetic method Methods 0.000 title claims abstract description 9
- 239000011701 zinc Substances 0.000 claims abstract description 38
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000002262 Schiff base Substances 0.000 claims abstract description 6
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 claims abstract description 5
- 230000003321 amplification Effects 0.000 claims abstract description 5
- 239000012153 distilled water Substances 0.000 claims abstract description 5
- 238000003199 nucleic acid amplification method Methods 0.000 claims abstract description 5
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000004246 zinc acetate Substances 0.000 claims abstract description 5
- 239000013078 crystal Substances 0.000 claims description 14
- JHZOXYGFQMROFJ-UHFFFAOYSA-N 3,5-dibromo-2-hydroxybenzaldehyde Chemical compound OC1=C(Br)C=C(Br)C=C1C=O JHZOXYGFQMROFJ-UHFFFAOYSA-N 0.000 claims description 9
- 238000005286 illumination Methods 0.000 claims description 7
- -1 4 triazole schiff bases Chemical class 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 claims description 4
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 claims description 4
- 230000001476 alcoholic effect Effects 0.000 claims description 4
- 238000004020 luminiscence type Methods 0.000 claims description 4
- 238000010992 reflux Methods 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- 238000005406 washing Methods 0.000 claims description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- 239000000126 substance Substances 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract 3
- FMCUPJKTGNBGEC-UHFFFAOYSA-N 1,2,4-triazol-4-amine Chemical compound NN1C=NN=C1 FMCUPJKTGNBGEC-UHFFFAOYSA-N 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- 238000011835 investigation Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002189 fluorescence spectrum Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
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- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/008—Supramolecular polymers
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1059—Heterocyclic compounds characterised by ligands containing three nitrogen atoms as heteroatoms
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/14—Macromolecular compounds
- C09K2211/1408—Carbocyclic compounds
- C09K2211/1425—Non-condensed systems
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
- C09K2211/1466—Heterocyclic containing nitrogen as the only heteroatom
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
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Abstract
The invention discloses a luminescent material [Zn(tibc)2]n and a synthetic method. The molecular formula of a monomer is C18H10ZnBr4N8O2; a molecular weight is 755.33g/mol; Htibc is 3,5-didibromosalicylidene-4-amino-1,2,4-triazole schiff base. Analytically pure 3,5-didibromosalicylaldehyde and analytically pure 4-amino-1,2,4-triazole are dissolved in an analytically pure ethanol solution; an obtained first mixture is heated, refluxed and agitated to obtain the ligand Htibc. The dried Htibc and analytically pure zinc acetate are dissolved in analytically pure N,N'-dimethyl formamide; distilled water is added into an obtained second mixture; an obtained third mixture is stood for five days in a drying oven at 90 DEG C. The [Zn(tibc)2]n generates 526.4nm fluorescent light with intensity of 529.7a.u. (astronomical unit) when being irradiated by 450nm incident light, and under an 800V photomultiplier and a 3 times of amplification coefficient, generates stable emergent light which has intensity of 2910a.u. when being put in a 1mol/L of potassium peroxodisulfate solution. The luminescent material [Zn(tibc)2]n and the synthetic method are simple in process, low in cost, easy in the control of chemical components, good in repeatability and further high in yield.
Description
Technical field
The present invention relates to a kind of stable luminescent material [Zn (tibc)2]n, (Htibc is 3,5-Dibromosalicylaldehyde contracting 4-amino-1,2,4 triazole schiff bases) and synthetic method。
Background technology
The development of many decades gone through by modern luminescent material, oneself become information show, the backing material in the field such as lighting source, photoelectric device, play the effect become more and more important for social development and technological progress。Particularly energy scarcity is present, and the luminescent material that exploitation transformation efficiency is high is to solve one of energy scarcity problem method。
Summary of the invention
The purpose of the present invention is exactly the functional material for design synthesis luminosity excellence, utilizes micro-bottle of reaction method synthesis [Zn (tibc)2]n。
[the Zn (tibc) that the present invention relates to2]nMolecular formula be: C18H10ZnBr4N8O2, molecular weight is: 755.33g/mol, Htibc are 3,5-Dibromosalicylaldehyde contracting 4-amino-1, and 2,4 triazole schiff bases, crystal structural data is in Table one, and bond distance's bond angle data are in Table two。
Table one: [Zn (tibc)2]nCrystallographic parameter
aR1=Σ | | Fo|–|Fc||/Σ|Fo|.bwR2=[Σ w (| Fo 2|–|Fc 2|)2/Σw(|Fo 2|)2]1/2
Table two: [Zn (tibc)2]nBond distanceWith bond angle °
| Zn1—O3 | 2.015(6) | N9—N17 | 1.367(10) |
| Zn1—O3i | 2.015(6) | N9—C10 | 1.313(10) |
| Zn1—N6 | 2.201(7) | N15—N6iii | 1.428(9) |
| Zn1—N6i | 2.201(7) | N15—C0AA | 1.360(11) |
| Zn1—N9 | 2.195(7) | N15—C10 | 1.321(11) |
| Zn1—N9i | 2.195(7) | N17—C0AA | 1.304(11) |
| Br5—C11 | 1.891(9) | C6—C7 | 1.422(14) |
| Br8—C16 | 1.894(11) | C6—C16 | 1.375(14) |
| O3—C5 | 1.282(10) | C7—C5 | 1.426(13) |
| N6—C8i | 1.279(11) | C5—C11 | 1.428(11) |
| N6—N15ii | 1.428(9) | C11—C20 | 1.358(14) |
| C8—N6i | 1.279(11) | C16—C20 | 1.395(15) |
| C8—C7 | 1.453(12) | ||
| O3—Zn1—O3i | 180.0(4) | C10—N9—N17 | 107.4(7) |
| O3—Zn1—N6i | 84.1(2) | C0AA—N15—N6iii | 126.9(7) |
| O3—Zn1—N6 | 95.9(2) | C10—N15—N6iii | 126.5(7) |
| O3i—Zn1—N6i | 95.9(2) | C10—N15—C0AA | 106.5(7) |
| O3i—Zn1—N6 | 84.1(2) | C0AA—N17—N9 | 107.3(7) |
| O3—Zn1—N9 | 87.9(3) | C16—C6—C7 | 119.8(10) |
| O3—Zn1—N9i | 92.1(3) | C6—C7—C8 | 115.1(8) |
| O3i—Zn1—N9i | 87.9(3) | C6—C7—C5 | 121.3(8) |
| O3i—Zn1—N9 | 92.1(3) | C5—C7—C8 | 123.6(8) |
| N6—Zn1—N6i | 179.999(1) | N17—C0AA—N15 | 109.0(8) |
| N9—Zn1—N6 | 95.1(3) | O3—C5—C7 | 124.5(7) |
| N9i—Zn1—N6i | 95.1(3) | O3—C5—C11 | 120.7(8) |
| N9—Zn1—N6i | 84.9(3) | C7—C5—C11 | 114.7(8) |
| N9i—Zn1—N6 | 84.9(3) | N9—C10—N15 | 109.8(7) |
| N9—Zn1—N9i | 180.0 | C5—C11—Br5 | 116.9(7) |
| C5—O3—Zn1 | 125.0(5) | C20—C11—Br5 | 119.1(7) |
| C8i—N6—Zn1 | 123.2(6) | C20—C11—C5 | 124.0(9) |
| C8i—N6—N15ii | 111.0(7) | C6—C16—Br8 | 120.6(9) |
| N15ii—N6—Zn1 | 122.3(5) | C6—C16—C20 | 120.5(10) |
| N6i—C8—C7 | 124.4(8) | C20—C16—Br8 | 118.8(8) |
| N17—N9—Zn1 | 123.0(5) | C11—C20—C16 | 119.6(9) |
| C10—N9—Zn1 | 129.5(6) |
Symmetrycodes:(i)-x ,-y+1 ,-z+1；(ii)-x, y-1/2 ,-z+3/2；(iii)-x, y+1/2 ,-z+3/2.
Described [Zn (tibc)2]nSynthetic method concretely comprise the following steps:
(1) by analytically pure for 2.79g 3,5-Dibromosalicylaldehyde and the analytically pure 4-amino-1 of 0.841g, 2,4-triazole, is dissolved in 30mL analytical pure alcoholic solution, is heated to reflux and has solid to precipitate out after stirring two hours, filter, by 10mL analytical pure washing with alcohol three times, dry at placing 50 DEG C, obtain part Htibc。Dried for 0.069-0.138g Htibc and 0.050-0.100g analytical pure zinc acetate is dissolved in 5mL analytical pure N, in N '-dimethyl Methanamide, it is placed in micro-reaction bulb, adds 5mL distilled water, 90 DEG C of baking ovens stand five days, has golden yellow crystal to generate i.e. [Zn (tibc)2]n。[Zn (tibc) is measured by single crystal diffractometer2]nStructure, crystal structural data is in Table one, and bond distance's bond angle data are in Table two。
(2) step (1) gained [Zn (tibc) is taken2]nBeing dissolved in analytical pure N, being made into concentration in N '-dimethyl formamide solvent is 5.0 × 10-6The solution of mol/L, carries out fluorometric investigation, [Zn (tibc)2]nThe fluorescence of the 526.4nm of 529.7a.u. intensity is produced under the incident illumination of 450nm irradiates；Under the photomultiplier tube of 800V, the amplification coefficient of 3 times, take the 100 above-mentioned solution prepared of μ L and be placed in 1mol/L potassium persulfate solution (conducting medium), create the luminescence of 2910a.u. intensity, and with this understanding, can continue and stabilized illumination。
The present invention has that technique is simple, with low cost, chemical constituent is easily controllable, reproducible and yield advantages of higher。
Accompanying drawing explanation
Fig. 1 is the present invention [Zn (tibc)2]nStructure chart。
Fig. 2 is the present invention [Zn (tibc)2]n2 d plane picture。
Fig. 3 is the present invention [Zn (tibc)2]nTomograph。
Fig. 4 is the present invention [Zn (tibc)2]nFluorescence spectrum figure。
Fig. 5 is the present invention [Zn (tibc)2]nElectrochemiluminescence spectrogram。
Detailed description of the invention
Embodiment 1:
[the Zn (tibc) that the present invention relates to2]nMolecular formula be: C18H10ZnBr4N8O2, molecular weight is: 755.33g/mol, Htibc are 3,5-Dibromosalicylaldehyde contracting 4-amino-1, and 2,4 triazole schiff bases, crystal structural data is in Table one, and bond distance's bond angle data are in Table two。
[Zn(tibc)2]nSynthetic method concretely comprise the following steps:
(1) by analytically pure for 2.79g 3,5-Dibromosalicylaldehyde and the analytically pure 4-amino-1 of 0.841g, 2,4-triazole, is dissolved in 30mL analytical pure alcoholic solution, is heated to reflux and has solid to precipitate out after stirring two hours, filter, by 10mL analytical pure washing with alcohol three times, dry at placing 50 DEG C, obtain part Htibc。Yield: 3.214g, productivity 94%。Dried for 0.069g Htibc and 0.050g analytical pure zinc acetate is dissolved in 5mL analytical pure N, in N '-dimethyl Methanamide, it is placed in micro-reaction bulb, adds 5mL distilled water, 90 DEG C of baking ovens stand five days, has golden yellow crystal to generate i.e. [Zn (tibc)2]n。Yield: 0.047g, productivity 47%。[Zn (tibc) is measured by single crystal diffractometer2]nStructure, crystal structural data is in Table one, and bond distance's bond angle data are in Table two。
(2) step (1) gained [Zn (tibc) is taken2]nBeing dissolved in analytical pure N, being made into concentration in N '-dimethyl formamide solvent is 5.0 × 10-5The solution of mol/L, carries out fluorometric investigation, [Zn (tibc)2]nThe fluorescence of the 526.4nm of 529.7a.u. intensity is produced under the incident illumination of 450nm irradiates；Under the photomultiplier tube of 800V, the amplification coefficient of 3 times, take the 100 above-mentioned solution prepared of μ L and be placed in 1mol/L potassium persulfate solution (conducting medium), create the luminescence of 2910a.u. intensity, and with this understanding, can continue and stabilized illumination。
Embodiment 2:
[the Zn (tibc) that the present invention relates to2]nMolecular formula be: C18H10ZnBr4N8O2, molecular weight is: 755.33g/mol, Htibc are 3,5-Dibromosalicylaldehyde contracting 4-amino-1, and 2,4 triazole schiff bases, crystal structural data is in Table one, and bond distance's bond angle data are in Table two。
[Zn(tibc)2]nSynthetic method concretely comprise the following steps:
(1) by analytically pure for 2.79g 3,5-Dibromosalicylaldehyde and the analytically pure 4-amino-1 of 0.841g, 2,4-triazole, is dissolved in 30mL analytical pure alcoholic solution, is heated to reflux and has solid to precipitate out after stirring two hours, filter, by 10mL analytical pure washing with alcohol three times, dry at placing 50 DEG C, obtain part Htibc。Yield: 3.214g, productivity 94%。Dried for 0.138g Htibc and 0.100g analytical pure zinc acetate is dissolved in 5mL analytical pure N, in N '-dimethyl Methanamide, it is placed in micro-reaction bulb, adds 5mL distilled water, 90 DEG C of baking ovens stand five days, has golden yellow crystal to generate i.e. [Zn (tibc)2]n。Yield: 0.094g, productivity 47%。[Zn (tibc) is measured by single crystal diffractometer2]nStructure, crystal structural data is in Table one, and bond distance's bond angle data are in Table two。
(2) step (1) gained [Zn (tibc) is taken2]nBeing dissolved in analytical pure N, being made into concentration in N '-dimethyl formamide solvent is 5.0 × 10-5The solution of mol/L, carries out fluorometric investigation, [Zn (tibc)2]nThe fluorescence of the 526.4nm of 529.7a.u. intensity is produced under the incident illumination of 450nm irradiates；Under the photomultiplier tube of 800V, the amplification coefficient of 3 times, take the 100 above-mentioned solution prepared of μ L and be placed in 1mol/L potassium persulfate solution (conducting medium), create the luminescence of 2910a.u. intensity, and with this understanding, can continue and stabilized illumination。
Claims (1)
1. a luminescent material [Zn (tibc)2]n, [the Zn (tibc) that the present invention relates to2]nMolecular formula be: C18H10ZnBr4N8O2, molecular weight is: 755.33g/mol, Htibc are 3,5-Dibromosalicylaldehyde contracting 4-amino-1, and 2,4 triazole schiff bases, crystal structural data is in Table one, and bond distance's bond angle data are in Table two；[Zn (tibc)2]nThe fluorescence of the 526.4nm of 529.7a.u. intensity is produced under the incident illumination of 450nm irradiates；Under the photomultiplier tube of 800V, the amplification coefficient of 3 times, it is placed in 1mol/L potassium persulfate solution, produces 2910a.u. intensity and stable luminescence；
Table one: [Zn (tibc)2]nCrystallographic parameter
aR1=Σ | | Fo|–|Fc||/Σ|Fo|.bwR2=[Σ w (| Fo 2|–|Fc 2|)2/Σw(|Fo 2|)2]1/2
Table two: [Zn (tibc)2]nBond distanceWith bond angle °
Symmetrycodes:(i)-x ,-y+1 ,-z+1；(ii)-x, y-1/2 ,-z+3/2；(iii)-x, y+1/2 ,-z+3/2.
Described [Zn (tibc)2]nSynthetic method concretely comprise the following steps:
(1) by analytically pure for 2.79g 3,5-Dibromosalicylaldehyde and the analytically pure 4-amino-1 of 0.841g, 2,4-triazole, is dissolved in 30mL analytical pure alcoholic solution, is heated to reflux and has solid to precipitate out after stirring two hours, filter, by 10mL analytical pure washing with alcohol three times, dry at placing 50 DEG C, obtain part Htibc；Dried for 0.069-0.138g Htibc and 0.050-0.100g analytical pure zinc acetate is dissolved in 5mL analytical pure N, in N '-dimethyl Methanamide, it is placed in micro-reaction bulb, adds 5mL distilled water, 90 DEG C of baking ovens stand five days, has golden yellow crystal to generate i.e. [Zn (tibc)2]n。
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Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102503963A (en) * | 2011-09-13 | 2012-06-20 | 江西师范大学 | Zinc metal-organic coordination polymer and preparation method thereof |
| JP2014152114A (en) * | 2013-02-05 | 2014-08-25 | Nippon Shokubai Co Ltd | Organometallic complex |
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102503963A (en) * | 2011-09-13 | 2012-06-20 | 江西师范大学 | Zinc metal-organic coordination polymer and preparation method thereof |
| JP2014152114A (en) * | 2013-02-05 | 2014-08-25 | Nippon Shokubai Co Ltd | Organometallic complex |
Non-Patent Citations (2)
| Title |
|---|
| MUHAMMAD HANIF等: "Design, spectral characterization and biological studies of transition metal(II) complexes with triazole Schiff bases", 《SPECTROCHIMICA ACTA PART A: MOLECULAR AND BIOMOLECULAR SPECTROSCOPY》 * |
| ZAHID H. CHOHAN等: "Synthesis and characterization of biologically active new Schiff bases containing 3-functionalized 1,2,4-triazoles and their zinc(II) complexes: crystal structure of 4-bromo-2-[(E)-(1H-1,2,4-triazol-3-ylimino)- methyl]phenol", 《APPL. ORGANOMETAL. CHEM.》 * |
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