Synthesis and characterization of new azobenzene-containing bis pentacyanoferrate(II) stoppered push–pull [2]rotaxanes, with α- and β-cyclodextrin. Towards highly medium responsive dyes
-
Add time:09/06/2019 Source:sciencedirect.com
The solvatochromic behavior of novel synthesized azo-containing viologen-based rotaxanes, combining push–pull linear and α or β-cyclodextrin macrocyclic components is examined. These rotaxanes are stoppered by pentacyanoferrate(II) units. The latter stabilize these systems and furthermore act as strong electron donors. These units are linked to strong electron withdrawing viologen units thus giving rise to an exceptionally intense solvatochromic behavior. Suitable solvent polarity scales and Linear Solvation Energy Relationships (LSERs) were employed in order to rationalize the solvent polarity effects observed, both specific and non-specific ones. The results for the title compounds as well as their Cyclodextrin-Free-Dumbbell (CFD) like analogue, are compared to recent published solvatochromic data regarding similar smaller pentacyanoferrate(II) complexes as well as other highly solvatochromic compounds. Structural effects on the solvatochromic intensity as well as the contribution of different solvent-solute interactions are rationalized and quantified.
We also recommend Trading Suppliers and Manufacturers of pentacyanoferrate (II) (cas 15699-35-1). Pls Click Website Link as below: cas 15699-35-1 suppliers
Prev:Solute-centric versus indicator-centric solvent polarity parameters in binary solvent mixtures. Determining the contribution of local solvent basicity to the solvatochromism of a pentacyanoferrate(II) dye☆
Next:Pentacyanoferrate(II) complexes with N-containing derivatives of chitosan and polyallylamine: Synthesis and cesium uptake properties) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Spectroscopic and substitution kinetic studies of pentacyanoferrate(II) complexes with sulphur heterocyclic ligands09/25/2019
- Regular paperMössbauer spectroscopic and thermal decomposition studies of alkylamine and nitrogen heterocyclic substituted pentacyanoferrate(II) complexes09/24/2019
- Acid–base and spectroscopic properties of a novel supramolecular porphyrin bonded to four pentacyanoferrate(II) groups09/10/2019
- Regular ArticleStoppering/unstoppering of a rotaxane formed between an N-hetorycle ligand containing surfactant: β-cyclodextrin pseudorotaxane and pentacyanoferrate(II) ions09/09/2019
- Preparation and characterization of the pentacyanoferrate(II) on the surface of N-(4-pyridilmethylidene)chitosan09/08/2019
- Pentacyanoferrate(II) complexes with N-containing derivatives of chitosan and polyallylamine: Synthesis and cesium uptake properties09/07/2019
- Solute-centric versus indicator-centric solvent polarity parameters in binary solvent mixtures. Determining the contribution of local solvent basicity to the solvatochromism of a pentacyanoferrate(II) dye☆09/05/2019
- Spectroscopic and structural insights into N-substituted pyridinium-4-aldoximes and their pentacyanoferrate(II) complexes09/04/2019
- Research paperRedox- and thermally-induced linkage isomerization of thieno[2,3-d]pyrimidin-4-one pentacyanoferrate(II/III) complexes09/03/2019


