Highly transparent polyimides derived from 2-phenyl-4, 6-bis(4-aminophenoxy)pyrimidine and 1, 3-bis(5-amino-2-pyridinoxy)benzene: preparation, characterization, and optical properties. Issue 125 (8th December 2015)
- Record Type:
- Journal Article
- Title:
- Highly transparent polyimides derived from 2-phenyl-4, 6-bis(4-aminophenoxy)pyrimidine and 1, 3-bis(5-amino-2-pyridinoxy)benzene: preparation, characterization, and optical properties. Issue 125 (8th December 2015)
- Main Title:
- Highly transparent polyimides derived from 2-phenyl-4, 6-bis(4-aminophenoxy)pyrimidine and 1, 3-bis(5-amino-2-pyridinoxy)benzene: preparation, characterization, and optical properties
- Authors:
- Wang, Chunbo
Guan, Yue
Tian, Dongbo
Dang, Guodong
Wang, Daming
Chen, Chunhai
Zhou, Hongwei - Abstract:
- Abstract : Heterocyclic polyimides were prepared from two novel diamines with anhydrides, which exhibit outstanding solubility and optical transparency properties. Abstract : To investigate the structure–property relationships of polyimides containing pyrimidine or pyridine moieties, two diamine monomers, 2-phenyl-4, 6-bis(4-aminophenoxy)pyrimidine and 1, 3-bis(5-amino-2-pyridinoxy)benzene, were designed and synthesized. The diamines reacted with different commercially available aromatic dianhydrides to yield a series of heterocyclic polyimides via a classical two-step polymerization method. The polyimides, PI-1 and PI-6, exhibited excellent solubility in strong polar solvents, such as N, N -dimethylacetamide, N, N -dimethylformamide and N -methyl-2-pyrrolidone. The flexible, strong and transparent polyimide films were formed with UV-visible absorption cut-off wavelengths at 344–399 nm. Glass transition temperatures ( T g ) of the polyimides PI-(1–6), derived from PBAPD and BADB with dianhydrides, in the range of 212–260 °C were obtained by DSC, and the temperatures for 5% wt loss of the polyimides in nitrogen and air atmospheres were obtained from TGA in the range of 430–503 °C and 422–465 °C, respectively. Moreover, the polyimide films showed a low moisture absorption of 0.18–1.38% and outstanding mechanical properties with tensile strengths of 81–111 MPa, an elongation at break of 4.3–8.7%, and a tensile modulus of 1.3–2.4 GPa. The coefficients of thermal expansion (CTEs)Abstract : Heterocyclic polyimides were prepared from two novel diamines with anhydrides, which exhibit outstanding solubility and optical transparency properties. Abstract : To investigate the structure–property relationships of polyimides containing pyrimidine or pyridine moieties, two diamine monomers, 2-phenyl-4, 6-bis(4-aminophenoxy)pyrimidine and 1, 3-bis(5-amino-2-pyridinoxy)benzene, were designed and synthesized. The diamines reacted with different commercially available aromatic dianhydrides to yield a series of heterocyclic polyimides via a classical two-step polymerization method. The polyimides, PI-1 and PI-6, exhibited excellent solubility in strong polar solvents, such as N, N -dimethylacetamide, N, N -dimethylformamide and N -methyl-2-pyrrolidone. The flexible, strong and transparent polyimide films were formed with UV-visible absorption cut-off wavelengths at 344–399 nm. Glass transition temperatures ( T g ) of the polyimides PI-(1–6), derived from PBAPD and BADB with dianhydrides, in the range of 212–260 °C were obtained by DSC, and the temperatures for 5% wt loss of the polyimides in nitrogen and air atmospheres were obtained from TGA in the range of 430–503 °C and 422–465 °C, respectively. Moreover, the polyimide films showed a low moisture absorption of 0.18–1.38% and outstanding mechanical properties with tensile strengths of 81–111 MPa, an elongation at break of 4.3–8.7%, and a tensile modulus of 1.3–2.4 GPa. The coefficients of thermal expansion (CTEs) of the polyimides ranged from 28 to 62 ppm °C −1 . … (more)
- Is Part Of:
- RSC advances. Volume 5:Issue 125(2015)
- Journal:
- RSC advances
- Issue:
- Volume 5:Issue 125(2015)
- Issue Display:
- Volume 5, Issue 125 (2015)
- Year:
- 2015
- Volume:
- 5
- Issue:
- 125
- Issue Sort Value:
- 2015-0005-0125-0000
- Page Start:
- 103246
- Page End:
- 103254
- Publication Date:
- 2015-12-08
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5ra19167j ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1380.xml