1999
DOI: 10.1080/10587259908023775
|View full text |Cite
|
Sign up to set email alerts
|

The Synthesis and Properties of Fluoroterphenyls for High Dielectric Biaxiality Ferroelectric Liquid Crystal Mixtures

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2005
2005
2022
2022

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 20 publications
(3 citation statements)
references
References 9 publications
0
3
0
Order By: Relevance
“…During the late 1980s and early 1990s, much research was conducted in the area of generating materials for ferroelectric applications, and one of the largest programmes involved the synthesis of ferroelectric host materials and chiral dopants to generate ferroelectric mixtures of high dielectric biaxiality [49][50][51][52][53][54][55][56]. In order to achieve this goal host materials of very high negative dielectric anisotropy were required, and this was best achieved by the use of materials with two lateral fluoro substituents inherently fixed on one side of the molecule (e.g., compound 47) [49].…”
Section: Chiral Induction In Mesophases Generated From Achiral and Ramentioning
confidence: 99%
“…During the late 1980s and early 1990s, much research was conducted in the area of generating materials for ferroelectric applications, and one of the largest programmes involved the synthesis of ferroelectric host materials and chiral dopants to generate ferroelectric mixtures of high dielectric biaxiality [49][50][51][52][53][54][55][56]. In order to achieve this goal host materials of very high negative dielectric anisotropy were required, and this was best achieved by the use of materials with two lateral fluoro substituents inherently fixed on one side of the molecule (e.g., compound 47) [49].…”
Section: Chiral Induction In Mesophases Generated From Achiral and Ramentioning
confidence: 99%
“…In a 500 ml previously dry-flamed three necked flask, 25 g (0.1244 mol) of compound 1 and 150 ml dried THF were mixed and stirred thoroughly. The system was then continuously purged with N 2 and placed in a dry-ice/ acetone bath, 278uC [23]. Into this flask 65 ml of 2.5 M BuLi (0.1625 mol) was added immediately but slowly through a dropping funnel.…”
Section: Synthesismentioning
confidence: 99%
“…The chalconyl derivatives, due to their geometrical shapes, may exhibit LC properties with lower thermometric transitions and bioactivity. The aims and objectives of this article are to study the effect of the molecular structure on the LC properties and behaviours [2][3][4][5][6] as a result of molecular flexibility, keeping the molecular rigidity unaltered throughout a series and changing their flexibility from series to series for the same homologue at constant rigidity. LC substances have proven their ability for LC devices to be operated at room temperature [7][8][9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%