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CAS RN: 917-23-7 | Product Number: T1359
Tetraphenylporphyrin (Chlorin free)
Purity: >98.0%(HPLC)
Synonyms:
- Tetraphenylporphine (Chlorin free)
- TPP (Chlorin free)
Product Documents:
Size | Unit Price | Shanghai | Tianjin | Japan* |
---|---|---|---|---|
1G |
¥470.00
|
2 | 3 | ≥60 |
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Product Number | T1359 |
Purity / Analysis Method | >98.0%(HPLC) |
Molecular Formula / Molecular Weight | C__4__4H__3__0N__4 = 614.75 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Air Sensitive |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
CAS RN | 917-23-7 |
Reaxys Registry Number | 379542 |
PubChem Substance ID | 87577126 |
MDL Number | MFCD00011680 |
Specifications
Appearance | Orange to Brown to Dark purple powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Tetraphenylchlorin | max. 0.5 % |
NMR | confirm to structure |
Properties (reference)
GHS
Related Laws:
Transport Information:
Customs Control Conditions (Q) |
Application
Molecular-weight Controlled Polymerization Using Aluminum-porphyrins
Typical Procedure:
The flask containing tetraphenylporphine ((TPP)H2)(1.0 mmol) is purged with dry N2, and then CH2Cl2 (20 mL) is introduced to dissolve (TPP)H2. To this solution is added Et2AlCl (1.2 mmol, 20% excess to (TPP)H2) by syringe under a N2 atmosphere at room temperature with stirring. After a definite time, the volatile materials are removed from this reaction mixture under reduced pressure to give a purple solid (TPP)AlCl) with metallic luster. CH2Cl2 (20 mL) is introduced to this flask to dissolve the product, to obtain the catalyst solution.
To the catalyst solution ((TPP)AlCl 20.4 mM) with stirring is added β-propiolactone (6.12 mol) by syringe at room temperature in a N2 atmosphere. After a definite time, a large excess of methanol is added to the reaction mixture to stop the polymerization, and then volatile materials are removed under reduced pressure to leave the product. The polymer is isolated as a slightly yellow-green powder by precipitation of the product from chloroform/methanol after shaking the chloroform solution with dilute hydrochloric acid.
The gel permeation chromatogram (GPC) of the resulting polymer shows the weight average molecular weight to the number average molecular weight (Mw/Mn) : 1.26 and the number average molecular weight (Mn) : 3500.
The flask containing tetraphenylporphine ((TPP)H2)(1.0 mmol) is purged with dry N2, and then CH2Cl2 (20 mL) is introduced to dissolve (TPP)H2. To this solution is added Et2AlCl (1.2 mmol, 20% excess to (TPP)H2) by syringe under a N2 atmosphere at room temperature with stirring. After a definite time, the volatile materials are removed from this reaction mixture under reduced pressure to give a purple solid (TPP)AlCl) with metallic luster. CH2Cl2 (20 mL) is introduced to this flask to dissolve the product, to obtain the catalyst solution.
To the catalyst solution ((TPP)AlCl 20.4 mM) with stirring is added β-propiolactone (6.12 mol) by syringe at room temperature in a N2 atmosphere. After a definite time, a large excess of methanol is added to the reaction mixture to stop the polymerization, and then volatile materials are removed under reduced pressure to leave the product. The polymer is isolated as a slightly yellow-green powder by precipitation of the product from chloroform/methanol after shaking the chloroform solution with dilute hydrochloric acid.
The gel permeation chromatogram (GPC) of the resulting polymer shows the weight average molecular weight to the number average molecular weight (Mw/Mn) : 1.26 and the number average molecular weight (Mn) : 3500.
References
- T. Aida, R. Mizuta, Y. Yoshida, S. Inoue, Makromol. Chem. 1981, 182, 1073.
- T. Yasuda, T. Aida, S. Inoue, Macromolecules 1984, 17, 2217.
- S. Asano, T. Aida, S. Inoue, J. Chem. Soc. Chem. Commun. 1985, 1148.
- Y. Watanabe, T. Yasuda, T. Aida, S. Inoue, Macromolecules 1992, 25, 1396.
- M. Komatsu, T Aida, S. Inoue, J. Am. Chem. Soc. 1991, 113, 8492.
- H. Sugimoto, M. Kuroki, T.Watanabe, C. Kawamura, T. Aida, S. Inoue, Macromolecules 1993, 26, 3403.
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