“…[1][2][3][4] From this standpoint, crown ether substituted fluoro-and chromophores capable of significant changes of photophysical properties upon selective binding of cations are of special interest. [5][6][7][8][9][10][11] Modification of the crown ether cycle allows achieving high selectivity and binding constants for biologically and environmentally important metal ions. For example, replacement of one or two oxygen atoms in this cycle by sulfur ones can lead to higher affinity for mercury and copper cations.…”
Section: Introductionmentioning
confidence: 99%
“…[12][13][14][15][16][17][18] Moreover, simultaneous inclusion of nitrogen atom into the crown-substituent of a coloured molecule as a part of both ionophoric and chromophoric moieties is an easy way to impart the chromoionophoric power to the dye molecule and obtain a spectral response to metal cation binding since their interaction with the nitrogen atom will reduce the overall chromophore conjugation and thus change the photophysical properties of the system. [5][6][7][8][9][10][11][19][20][21][22][23] In this regard, aza-crown substituted hemicyanines represent one of the most promising compounds for sensory applications due to the combination of hemicyanine spectral properties (absorbance and fluorescence in visible range), crown ether receptor ability and ease of chemical modification. [5,12,17,[24][25][26][27][28][29][30][31][32] However, most studies concerning the sensory properties of such crown-substituted hemicyanines were done in solution.…”
Planar supramolecular systems based on Langmuir monolayers of chromoionophores are widely used for sensor applications, and crown ether ionophoric groups are intensively studied. However, almost no attention is devoted to investigation of effect of alkyl moieties onto receptor properties of such systems. In the present work, we carry out a comparative study of Langmuir monolayers of three alkylated dithiaaza-crown substituted hemicyanine chromoionophores differing only in number of carbon atoms (12,16,21)
“…[1][2][3][4] From this standpoint, crown ether substituted fluoro-and chromophores capable of significant changes of photophysical properties upon selective binding of cations are of special interest. [5][6][7][8][9][10][11] Modification of the crown ether cycle allows achieving high selectivity and binding constants for biologically and environmentally important metal ions. For example, replacement of one or two oxygen atoms in this cycle by sulfur ones can lead to higher affinity for mercury and copper cations.…”
Section: Introductionmentioning
confidence: 99%
“…[12][13][14][15][16][17][18] Moreover, simultaneous inclusion of nitrogen atom into the crown-substituent of a coloured molecule as a part of both ionophoric and chromophoric moieties is an easy way to impart the chromoionophoric power to the dye molecule and obtain a spectral response to metal cation binding since their interaction with the nitrogen atom will reduce the overall chromophore conjugation and thus change the photophysical properties of the system. [5][6][7][8][9][10][11][19][20][21][22][23] In this regard, aza-crown substituted hemicyanines represent one of the most promising compounds for sensory applications due to the combination of hemicyanine spectral properties (absorbance and fluorescence in visible range), crown ether receptor ability and ease of chemical modification. [5,12,17,[24][25][26][27][28][29][30][31][32] However, most studies concerning the sensory properties of such crown-substituted hemicyanines were done in solution.…”
Planar supramolecular systems based on Langmuir monolayers of chromoionophores are widely used for sensor applications, and crown ether ionophoric groups are intensively studied. However, almost no attention is devoted to investigation of effect of alkyl moieties onto receptor properties of such systems. In the present work, we carry out a comparative study of Langmuir monolayers of three alkylated dithiaaza-crown substituted hemicyanine chromoionophores differing only in number of carbon atoms (12,16,21)
“…Several general synthetic approaches to the preparation of discrete metallacycles have emerged, which include directional bonding [46,47], symmetry interactions [48,49], and weak-link approaches [50]. Many impressive examples of metallosupramolecular materials can be found in studies reported by Lehn [1,49,70], Sauvage [51], Stang [46,47], Fujita [26][27][28][29][30][31], Mirkin [50], Hupp [52][53][54][55], Lees [56][57][58][59], Lu [60,61], Jin [62,63], and others [64][65][66][67]. Lehn et al demonstrated the spontaneous self-assembly of dinuclear helicates from bipyridine and copper (I) [70].…”
“…As well, dendrimers can be constructed using linear building blocks, where branching centers are created during generational growth. Dendrimers have been examined in a numerous applications, including chemical (Kumar et al, 2008;Park et al, 2009) and electrical sensing, (Koo et al, 2001) micellar host-guest ability (Boisselier et al, 2010), coatings and polymer additives (Hartmann-Thompson et al, 2009), and drug delivery vehicles .…”
The advent of dendritic chemistry has facilitated materials research by allowing precise control of functional component placement in macromolecular architecture. The iterative synthetic protocols used for dendrimer construction were developed based on the desire to craft highly branched, high molecular weight, molecules with exact mass and tailored functionality. Arborols, inspired by trees and precursors of the utilitarian macromolecules known as dendrimers today, were the first examples to employ predesigned, 1 → 3 C-branched, building blocks; physical characteristics of the arborols, including their globular shapes, excellent solubilities, and demonstrated aggregation, combined to reveal the inherent supramolecular potential (e.g., the unimolecular micelle) of these unique species. The architecture that is a characteristic of dendritic materials also exhibits fractal qualities based on self-similar, repetitive, branched frameworks. Thus, the fractal design and supramolecular aspects of these constructs are suggestive of a larger field of fractal materials that incorporates repeating geometries and are derived by complementary building block recognition and assembly. Use of terpyridine-M2+-terpyridine (where, M = Ru, Zn, Fe, etc) connectivity in concert with mathematical algorithms, such as forms the basis for the Seirpinski gasket, has allowed the beginning exploration of fractal materials construction. The propensity of the fractal molecules to self-assemble into higher order architectures adds another dimension to this new arena of materials and composite construction.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.