Synthesis and characterization of poly (2,5-diyl pyrrole-2-pyrrolyl methine) semiconductor copolymer
Creators
- 1. Laboratoire de chimie Organique, Macromoléculaire et des Matériaux (LCOMM), Université de Mascara, Faculté des Sciences Exactes, BP 763 Mascara 29000 (Algeria)
- 2. Laboratoire de Chimie Physique des Macromolécules et Interfaces Biologiques, Université de Mascara Algeria (Algeria)
- 3. Laboratoire de Génie Physique, Université d'Ibn Khaldoun, Tiaret BP 78 14000 Tiaret (Algeria)
- 4. Mechanical Engineering Department, College of Engineering, United Arab Emirates University, Al-Ain (United Arab Emirates)
Description
The proposed technique to synthesise poly {(2,5-diyl pyrrole) (2-pyrrolyl methine)} (PPPM) copolymer by condensation of pyrrole and pyrrole-2-carboxaldehyde monomers catalyzed by Maghnite-H+ is introduced. The protons are exchanged with Maghnite-H+, which is available in the form of a montmorillonite silicate clay sheet. The effect of several parameters such as time and temperature of copolymerization, [pyrrole]/[pyrrole-2-carboxaldehyde] molar ratio, amount of Maghnite-H+, and solvent on the produced poly (2,5-diyl pyrrole-2-pyrrolyl methine) semiconductor copolymer material (yield%) was investigated. The synthesized PPPM copolymer was characterized using nuclear magnetic resonance, Fourier transform infrared, and ultraviolet–visible spectroscopy. The results show that the synthesized copolymer using the copolymerization technique is a real organic copolymer consisting of two monomers units (i.e, pyrrole and pyrrole-2-carboxaldehyde). Also, the synthesized copolymer is more soluble than polypyrrole in most of the commonly used organic solvents. Hence, copolymerization of pyrrole with pyrrole-2-carboxaldehyde will overcome the insolubility of polypyrrole. In addition, the resultant copolymer exhibits good film formability. The produced copolymer has several potential applications in the field of rechargeable batteries, sensors, capacitors, light emitting diodes, optical displays, and solar cells. (paper)
Availability note (English)
Available from http://dx.doi.org/10.1088/1674-4926/39/10/102001Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Semiconductors
- Journal Volume
- 39
- Journal Issue
- 10
- Journal Page Range
- [7 p.]
- ISSN
- 1674-4926
INIS
- Country of Publication
- China
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 51067340
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- COPOLYMERIZATION; COPOLYMERS; FOURIER TRANSFORMATION; LIGHT EMITTING DIODES; MONTMORILLONITE; NUCLEAR MAGNETIC RESONANCE; ORGANIC SOLVENTS; PYRROLES; SEMICONDUCTOR MATERIALS; SENSORS; SOLAR CELLS; ULTRAVIOLET RADIATION
- Descriptors DEC
- AZOLES; CHEMICAL REACTIONS; CLAYS; DIRECT ENERGY CONVERTERS; ELECTROMAGNETIC RADIATION; EQUIPMENT; HETEROCYCLIC COMPOUNDS; INORGANIC ION EXCHANGERS; INTEGRAL TRANSFORMATIONS; ION EXCHANGE MATERIALS; MAGNETIC RESONANCE; MATERIALS; MINERALS; NONAQUEOUS SOLVENTS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC POLYMERS; PHOTOELECTRIC CELLS; PHOTOVOLTAIC CELLS; POLYMERIZATION; POLYMERS; RADIATIONS; RESONANCE; SEMICONDUCTOR DEVICES; SEMICONDUCTOR DIODES; SILICATE MINERALS; SOLAR EQUIPMENT; SOLVENTS; TRANSFORMATIONS