Organic metal iridium complex and application thereof
An iridium complex, organometallic technology, applied in indium organic compounds, platinum group organic compounds, organic chemistry, etc., can solve the problems of poor carrier transport ability, affecting product quality and commercial competitiveness, high cost, etc. The effect of maintaining film stability, good industrialization prospects, and avoiding aggregation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] Embodiment 1: the synthesis of compound 1
[0043]
[0044] In a 150mL three-necked flask, add 0.02mol of 2-phenylpyridine, 3g (0.01mol) of IrCl 3(iridium trichloride), 60 mL of ethylene glycol ether, 30 mL of distilled water, nitrogen protection, heated to 120 ° C, reflux for 24 hours, then stopped the reaction, and naturally cooled to room temperature. Add 80mL of 1mol / L dilute hydrochloric acid, stir evenly, filter, the filter cake is rinsed 3 times with distilled water, then rinsed 2 times with absolute ethanol, and vacuum-dried to obtain dark green intermediate B1. Mass spectrometry analyzes its molecular weight to be 1136.10 (C 44 h 32 Cl 2 Ir 2 N 4 ). The elemental analysis results are: C, 49.25; H, 3.03; N, 5.25; the theoretical values are: C, 49.29; H, 3.01; N, 5.23.
[0045] In a 150mL three-necked flask, add 0.005mol intermediate B1, 0.01mol compound C1, 0.015mol sodium carbonate (Na 2 CO 3 ), 100 mL of ethylene glycol ether, under nitrogen prot...
Embodiment 2
[0047] Embodiment 2: the synthesis of compound 10
[0048]
[0049] In a 150mL three-necked flask, add 0.02mol of compound A2, 3g (0.01mol) of IrCl 3 (iridium trichloride), 60ml of ethylene glycol ether, 30mL of distilled water, nitrogen protection, heated to 120 ° C, reflux reaction for 24 hours, then stop the reaction, naturally cooled to room temperature. Add 80mL of 1mol / L dilute hydrochloric acid, stir evenly, filter, filter cake is rinsed 3 times with distilled water, then rinsed 2 times with absolute ethanol, and vacuum-dried to obtain dark green intermediate B2. According to mass spectrometry, its molecular weight is 1432.60 (C 72 h 56 Cl 2 Ir 2 N 4 ). The elemental analysis results are: C, 60.41; H, 3.95; N, 3.89; the theoretical values are: C, 60.37; H, 3.94; N, 3.91.
[0050] In the 150mL three-necked flask, add 0.005mol intermediate B2, 0.01mol compound C2, 0.015mol sodium carbonate (Na 2 CO 3 ), 100 mL of ethylene glycol ether, under nitrogen protect...
Embodiment 3
[0052] Embodiment 3: the synthesis of compound 20
[0053]
[0054] In a 150mL three-necked flask, add 0.02mol of compound A3, 3g (0.01mol) of IrCl 3 (iridium trichloride), 60ml of ethylene glycol ether, 30mL of distilled water, nitrogen protection, heated to 120 ° C, reflux reaction for 24 hours, then stop the reaction, naturally cooled to room temperature. Add 80mL of 1mol / L dilute hydrochloric acid, stir evenly, filter, filter cake is rinsed 3 times with distilled water, then rinsed 2 times with absolute ethanol, and vacuum-dried to obtain dark green intermediate B3. Mass spectrometry analysis showed that its molecular weight was 1600.93 (C 84 h 80 Cl 2 Ir 2 N 4 ). The elemental analysis results are: C, 66.10; H, 5.08; N, 3.46; the theoretical values are: C, 63.02; H, 5.04; N, 3.50.
[0055] In a 150mL three-necked flask, add 0.005mol intermediate B3, 0.01mol compound C2, 0.015mol sodium carbonate (Na 2 CO 3 ), 100mL of ethylene glycol ether, under nitrogen pr...
PUM
Property | Measurement | Unit |
---|---|---|
Film thickness | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com