Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

A New Series of Two-Ring-Based Side Chain Liquid Crystalline Polymers: Synthesis and Mesophase Characterization

Goddeti Siva Mohan Reddy A B E , Tanneru Narasimhaswamy C E , Jarugala Jayaramudu B , Emmanuel Rotimi Sadiku B , Konduru Mohana Raju A and Suprakas Sinha Ray D
+ Author Affiliations
- Author Affiliations

A Department of Polymer Science and Technology, Sri Krishnadevaraya University, Anantapur, 515003, India.

B Chemical, Metallurgical and Material Engineering, Polymer Technology Division, Tshwane University of Technology, Pretoria 0001, South Africa.

C Polymer Division, Council of Scientific and Industrial Research - Central Leather Research Institute, Adyar, Chennai, 600020, India.

D DST/CSIR National Centre for Nano-structured Materials, Council for Scientific and Industrial Research, Pretoria 0001, South Africa.

E Corresponding authors. Email: smreddyg@gmail.com, tnswamy99@hotmail.com

Australian Journal of Chemistry 66(6) 667-675 https://doi.org/10.1071/CH13090
Submitted: 22 February 2013  Accepted: 15 March 2013   Published: 27 May 2013

Abstract

A new series of side chain liquid crystalline polymers containing a core, a butamethylenoxy spacer, ester groups, and terminal alkoxy groups were synthesised and their structures were confirmed. The core was constructed with two phenyl rings and an ester linking unit. All the polymers were characterised by hot-stage polarising optical microscopy, differential scanning calorimetry, variable temperature X-ray diffraction, thermogravimetric analysis, and gel permeation chromato-graphy. The polymers were found to be liquid crystalline. The nematic and smectic A (SA) phases were observed for the homologues with short-terminal chains (C2 and C6), whereas the homologues with longer chains (C8 to C12) exhibited a smectic C phase. The thermal stability of the polymers was found to be in the range of 293 to 326°C and the molecular weights of the polymers were found to vary from 6 × 103 to 1.3 × 104.


References

[1]  X. Wang, Q. Zhou, Liquid Crystalline Polymers 2004 (World Scientific Publishing Co.: Singapore).

[2]  S. Poser, H. Fisher, M. Arnold, Prog. Polym. Sci. 1998, 23, 1337.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXnsFOmtLo%3D&md5=43b68d48b234c88240d661866152be19CAS |

[3]  W. Kreuder, O. W. Webster, H. Ringsdorf, Makromol. Chem., Rapid. Commun. 1986, 7, 5.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL28XhtFShtbY%3D&md5=f1846b134f3622ac8af328471e5dfadcCAS |

[4]  H. Finkelmann, H. Ringsdorf, J. H. Wendorf, Makromol. Chem. 1978, 179, 273.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE1cXhtlOjtLg%3D&md5=ed5f65dbca9637fda65e658c98f410e8CAS |

[5]  H. Finkelmann, Polymer Liquid Crystals 1982 (Academic Press: New York, NY).

[6]  N. A. Platé, V. P. Shibaev, Makromol. Chem. Suppl. 1984, 6, 3.
         | Crossref | GoogleScholarGoogle Scholar |

[7]  V. P. Shibaev, N. A. Plate, Pure Appl. Chem. 1985, 57, 1589.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL28XjsVemsw%3D%3D&md5=781d18d71d259cd818b4858e84d8ced3CAS |

[8]  C. Noël, P. Navarad, Prog. Polym. Sci. 1991, 16, 55.
         | Crossref | GoogleScholarGoogle Scholar |

[9]  H. A. Jacobs, G. M. Day, W. R. Jackson, G. P. Simmon, K. G. Watson, S. Zheng, Aust. J. Chem. 1992, 45, 695.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK38XisVGltr8%3D&md5=8abfd99f7f07bfe45bcbc33069c3af01CAS |

[10]  M. Portugall, H. Ringsdorf, R. Zentel, Makromol. Chem. 1982, 183, 2311.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3sXkvVCm&md5=22d2e709f9d80acaf1079d42e1f7be33CAS |

[11]  Y. B. Amerik, B. A. Krentsel, J. Polym. Sci., Part C: Polym. Symp. 1967, 16, 1383.
         | Crossref | GoogleScholarGoogle Scholar |

[12]  F. M. Hermay, Encyclopedia of Polymers and Engineering, 2nd edn, Vol. 9 1987 (John Wiley & Sons: New York, NY).

[13]  Y. K. Godovsky, V. S. Papkov, Adv. Polym. Sci. 1989, 88, 129.
         | Crossref | GoogleScholarGoogle Scholar |

[14]  E. Perplies, H. Ringsdorf, J. H. Wendorff, Makromol. Chem. 1974, 175, 553.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE2cXltVKjtLs%3D&md5=292f4467a72e53cd1511786320b747c3CAS |

[15]  V. N. Tsvetkov, E. I. Riumtsev, I. N. Shetennikova, E. V. Korneeva, B. A. Krenstel, A. Turner-Jones, Eur. Polym. J. 1973, 9, 481.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE3sXksl2gtb0%3D&md5=b97f0d220a5158d516a2b1f62269ac7bCAS |

[16]  I. A. Borthwick, J. M. W. Cowie, Polym. Adv. Technol. 1998, 9, 128.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXhs1Cksrg%3D&md5=e1155a5766e7f7dfb06ad7a3fcfac38dCAS |

[17]  J. H. Liu, P. C. Yang, Y. H. Chiu, Y. Suda, J. Polym. Sci., Part A: Polym. Chem. 2007, 45, 2026.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXltFCgur8%3D&md5=66e49a08c3221a7e97c0afb39efa5454CAS |

[18]  R. Lorenz, Liq. Cryst. 1989, 6, 667.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3cXktVKru7k%3D&md5=b47a529efc37c32d8ad46ef06152a0dbCAS |

[19]  R. Lorenz, Liq. Cryst. 1991, 9, 127.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXhtVaqsLo%3D&md5=f8f6dd46c58a3d97c55cc22ac790f5b9CAS |

[20]  A. Shanavas, T. Narasimhaswamy, A. S. Nasar, Aust. J. Chem. 2012, 65, 1426.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhsFersL7P&md5=943d387e8ffaee017d96a8414e8a5380CAS |

[21]  F. V. Pereira, R. Borsali, O. M. S. Ritter, P. F. Gonçalves, A. A. Merlo, N. P. da Silveira, J. Braz. Chem. Soc. 2006, 17, 333.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XjsFCnt7s%3D&md5=5097b45b8065520e5c268fdf52cdea67CAS |

[22]  A. De Vries, Mol. Cryst. Liq. Cryst. 1985, 131, 125.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2MXmt1Cms7w%3D&md5=bd69d28cc569e76c838007585296f249CAS |

[23]  J. Frenzel, G. Rehage, Makromol. Chem. 1983, 184, 1685.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3sXlsVSksLk%3D&md5=4e30e0047b96327325aafd6ed94d0269CAS |

[24]  P. J. Kocienski, Protecting Groups, 3rd edn 2005 (Georg Thieme: Stuttgart).

[25]  W. Greene, Protecting Groups in Organic Synthesis 2007 (John Wiley & Sons: New York, NY).

[26]  K. E. Rowe, D. W. Bruce, J. Mater. Chem. 1998, 8, 331.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXmslOjtw%3D%3D&md5=253bfcf094890b1847f8aa899304af84CAS |