Metallomesogens 1995
DOI: 10.1002/9783527615094.ch3
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Low Molecular Weight Calamitic Metallomesogens

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Cited by 8 publications
(9 citation statements)
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“…β-Diketones are key precursors for the synthesis of various five-membered heterocyclic and metallomesogenic derivatives. [2] The presence of hetero atoms such as N, O and S causes significant effects on dipole moment, polarisability and electronic nature of the molecules. Therefore, a large number of liquid crystals (LCs) have been derived from these heterocyclic cores.…”
Section: Introductionmentioning
confidence: 99%
“…β-Diketones are key precursors for the synthesis of various five-membered heterocyclic and metallomesogenic derivatives. [2] The presence of hetero atoms such as N, O and S causes significant effects on dipole moment, polarisability and electronic nature of the molecules. Therefore, a large number of liquid crystals (LCs) have been derived from these heterocyclic cores.…”
Section: Introductionmentioning
confidence: 99%
“…4,21 According to the literature mentioned above and Schiff base (azomethine) has been widely utilized as a linking group in the synthesis of many types of LC molecules. 22 Its derivative, salicylaldimine[N-(2-hydroxy-4-alkoxybenzylidene) aniline], possesses a quasi-six-membered ring resulting from intramolecular hydrogen (H)-bonding between the H-atom of the hydroxy group and the nitrogen (N)-atom of the imine linkage and thus exhibits more stability to moisture and heat than that of Schiff base analogues. With their synthetic versatility and ability to coordinate metals, they have also been applied in metallomesogens.…”
Section: Introductionmentioning
confidence: 99%
“…In these surfactants, the metal complex entity containing the central metal ion with its primary coordination sphere, acts as the head group and the hydrophobic entity of one or more ligands acts as the tail part. Surfactant metal complexes are expected to provide a wide range of interesting phenomena on aggregation in aqueous solution due to variations in charge numbers, size and extent of hydrophobicity through combination of the central metal and ligands [16]. The biological active compounds generally become more bacteriostatic and carcinostatic upon chelation with metal ions [17].…”
Section: Introductionmentioning
confidence: 99%