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Wyświetlanie pozycji 1-9 z 9
How much do coulombic interactions stabilize a mesophase? Ion pair and non-ionic binary isosteric derivatives of monocarbaborates and carboranes
(Royal Society of Chemistry, 2014)
Replacement of the B− atom in the monocarbaborate anion, 1[10] or 1[12], and the N^+ atom in the pyridinium cation [Pyr] of a liquid crystalline ion pair with C atoms leads to an isoelectronic and isosteric non-ionic binary ...
Investigation of high Δε derivatives of the [closo-1- CB_9H_10] anion for liquid crystal display applications
(Royal Society of Chemistry, 2014)
Two series of polar compounds 3[n] and 4[n] with longitudinal dipole moments ranging from 10 to 17 D were synthesized and investigated as additives to two nematic hosts, ClEster and CinnCN. Compounds 3[n] do not exhibit ...
Zwitterionic pyridinium derivatives of [closo-1-CB_9H_10]− and [closo-1-CB_11H_12]− as high Δε additives to a nematic host
(Royal Society of Chemistry, 2013)
Substituted closo-carbaborate–pyridinium zwitterions were prepared in 35–50% yield by reacting 1-amino-closo-1-carbaborates with 4-alkoxypyrylium triflates. Two of the new materials, 1[6]d and 2[10]b, exhibit a high ...
Liquid crystalline radicals: discotic behavior of unsymmetrical derivatives of 1,3,5-triphenyl-6-oxoverdazyl
(The Royal Society of Chemistry, 2013)
A series of six 6-oxoverdazyl (1[10]) substituted with a total of three 3,4,5-tri(decyloxy)phenyl and/or 3,4,5-tri(decylsulfanyl)phenyl groups was investigated by thermal, XRD, spectroscopic, magnetic and photovoltaic ...
3‑Substituted Benzo[e][1,2,4]triazines: Synthesis and Electronic Effects of the C(3) Substituent
(American Chemical Society, 2019)
A series of 19 structurally diverse C(3)-substituted derivatives of benzo[e][1,2,4]triazine were synthesized from 3-chloro- (1c) and 3-iodobenzo[e][1,2,4]triazine (1d) obtained in three steps from 2-nitroaniline in 37–55% ...
Axially Chiral Stable Radicals: Resolution and Characterization ofBlatter Radical Atropisomers
(American Chemical Society, 2021-09-17)
Atropisomers of three Blatter radicals were obtainedby the addition of 8-substituted 1-naphthyllithiums to 3-phenyl and3-t-butylbenzo[e][1,2,4]triazine and separated by chiral high-performance liquid chromatography. Their ...
3-Substituted Blatter Radicals: Cyclization of N-Arylguanidines and N-Arylamidines to Benzo[e][1,2,4]triazines and PhLi Addition
(American Chemical Society, 2023-02-17)
A series of 3-amino- and 3-alkyl-substituted 1-phenyl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yls was prepared in four steps involving N-arylation, cyclization of N-arylguanidines and N-arylamidines, reduction of the resulting ...
[closo-B10H8-1,10-(COOH)2]2−: a building block for functional materials?
(Royal Society of Chemistry Journals, 2021-12-15)
[closo-B10H8-1,10-(COOH)2]2− was obtained in five steps and 40% overall yield from [closo-B10H10]2−. It can be converted to [closo-B10H8-1,10-(CO)2] and subsequently to carbonium ylides [closo-B10H8-1-COOH-10-(C(NRCH2)2)]. ...
A photo-Smiles rearrangement: Mechanistic investigation of the formation of Blatter radical helicenes
(ACS, 2025-01-10)
Photocyclization of 8-aryloxy-3-phenylbenzo[e]-
[1,2,4]triazines leads to helicene radicals. Structural analysis of
radicals leuco forms by two-dimensional correlation nuclear
magnetic resonance methods demonstrated ...