2012
DOI: 10.6060/mhc2012.121106s
|View full text |Cite
|
Sign up to set email alerts
|

Two-Dimensional Aggregation of Crown-Phthalocyanine Ligand at Air-Water Interface

Abstract: Physico-chemical properties of monolayers of tetra-15-crown-5-phthalocyanine ligand were studied using Langmuir-

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2015
2015
2022
2022

Publication Types

Select...
6

Relationship

1
5

Authors

Journals

citations
Cited by 6 publications
(3 citation statements)
references
References 32 publications
0
3
0
Order By: Relevance
“…Considering the fact that CRPcRu(pyz) 2 bears two axial pyrazine ligands, which are quite hydrophilic, face-on orientation of the molecule is most likely. The observed discrepancy between the experimental molecular area and the theoretical one is commonly explained by hydrophilic and labile nature of the crown-ether moieties, which can be partially immersed into the aqueous subphase and/or deformed slightly in the monolayer [ 36 , 37 , 38 , 39 ].…”
Section: Resultsmentioning
confidence: 99%
“…Considering the fact that CRPcRu(pyz) 2 bears two axial pyrazine ligands, which are quite hydrophilic, face-on orientation of the molecule is most likely. The observed discrepancy between the experimental molecular area and the theoretical one is commonly explained by hydrophilic and labile nature of the crown-ether moieties, which can be partially immersed into the aqueous subphase and/or deformed slightly in the monolayer [ 36 , 37 , 38 , 39 ].…”
Section: Resultsmentioning
confidence: 99%
“…The method that has been devel oped makes it possible to control of the state of mono layer on aqueous subphase directly in the process of its formation and compression. For example, interrela tion between concentration of the solution, from which the monolayer was formed, and aggregation degree of the phthalocyanine ligand was determined using this method [167]. This allowed us to confirm that the absence of aggregation in the forming solution does not guarantee the absence of aggregation on the surface of aqueous subphase, and only with the use of relatively diluted solutions one can obtain true mono layers of the compound.…”
Section: Langmuir Monolayers and Langmuir-blodgett Films -Basic Ideasmentioning
confidence: 94%
“…Later, it was used to determine the number of molecules in aggregates of the crown-phthalocyanine ligand on the surface of water and by other authors. [22] Thin films of corroles possess peculiar structural and photophysical properties, making them candidates for application as photosensitizers, electronic molecular devices, etc. [23][24][25][26] Corroles (H 3 Cor) compared to porphyrins (H 2 P), have a wider variety of macrocyclic structures and high reactivity.…”
Section: Introductionmentioning
confidence: 99%