2020
DOI: 10.1016/j.molliq.2020.112693
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Pyrimidine-based ferroelectric mixtures – The influence of oligophenyl based chiral doping system

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Cited by 17 publications
(8 citation statements)
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“…From the obtained results [37], many interesting conclusions regarding the influence of the chiral dopants structure on the properties of final multicomponent FLC mixtures can be highlighted. Some of the physicochemical and electro-optical parameters of prepared mixtures described in Ref.…”
mentioning
confidence: 89%
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“…From the obtained results [37], many interesting conclusions regarding the influence of the chiral dopants structure on the properties of final multicomponent FLC mixtures can be highlighted. Some of the physicochemical and electro-optical parameters of prepared mixtures described in Ref.…”
mentioning
confidence: 89%
“…In order to obtain FLCs material according to the idea of doping achiral mixture with chiral dopant, the bicyclic pyrimidine compounds with alkyl or/and alkoxy terminal chain (based on a general structure 1, where: R 1 and R 2 are C n H 2n+1 -or C n H 2n+1 O-; n = 4 ÷11) were chosen and an achiral base mixture (denoted here as W) was prepared [37].…”
Section: Flcs Prepared From Achiral Smc Basic Mixture and Chiral Dopantsmentioning
confidence: 99%
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“…However, each part of the reactive mesogen molecule, namely the molecular core, type and position of the lateral substitution, linkage groups, length and type of the flexible chains, etc., can significantly change the resulting self-assembling behaviour of the designed material. The methyl [ 10 , 22 , 38 , 39 ] and methoxy [ 39 , 40 , 41 ] groups and halogen atoms [ 38 , 42 ], namely fluorine [ 42 , 43 , 44 , 45 , 46 , 47 ], chlorine [ 38 , 41 , 42 , 46 , 48 , 49 ], bromine [ 38 , 43 ] and iodine [ 50 ], are the most widely used and successful types of lateral substituents utilised for the effective tuning of the self-assembling behaviour, especially for the non-chiral and chiral calamitic LC materials. The type and position of the lateral substituents on the molecular core always drastically change the liquid crystalline behaviour of the resulting LC material when compared with its non-substituted analogue [ 38 , 39 ].…”
Section: Introductionmentioning
confidence: 99%
“…Lateral substitution as effective tool for tuning self-organising behaviour of chiral mesogens ≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡≡ However, during last decades of intense research, it has been shown that to reach the desired specific mesomorphic and electro-optical properties in a single molecular structure is almost impossible. This problem can be solved by the design of binary and multicomponent mixtures composed by structurally similar [7][8][9][10] or structurally different [11][12][13][14] molecules mixed-up in a definite quantity. Incorporation of various polymerisable groups, for example vinyl [15][16], acrylate [17][18][19][20][21], methacrylate [22][23][24], or various functional photoactive moieties (azo group [16][17], cinnamoyl group [27], hydrazone [28], spiropyrane [29], etc.)…”
Section: Introductionmentioning
confidence: 99%