4.6 Article

Recognition of dicarboxylate anions by a ditopic hexaazamacrocycle containing bis-p-xylyl spacers

Journal

NEW JOURNAL OF CHEMISTRY
Volume 30, Issue 2, Pages 247-257

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b512661d

Keywords

-

Ask authors/readers for more resources

The hexaprotonated form of the hexaazamacrocycle, 7,22-dimethyl-3,7,11,18,22,26-hexaazatricyclo[26.2.2.2.13.16]tetratriaconta-1(30), 13 15,28,31,33-hexaene, (H6Me2[30]pbz(2)N(6))(6+), was used as a receptor for the molecular recognition of aliphatic and aromatic carboxylate Substrates. The receptor-substrate binding behaviour of (H6Me2[30]pbz(2)N(6))(6+) With aliphatic >O--(2)(CH2)(n)CO2-, n=0 to 4] and aromatic (benzoate, phthalate, isophthalate, and terephthalate) Substrates Was evaluated by potentiometry and H-1 NMR spectroscopy. The association constants of the entities formed were determined in H2O at 298.0 K and 0.1 M KNO3 (by potentiometry) and in D2O (by H-1 NMR). The constants for the aliphatic Substrates are much lower than for the aromatic ones. NMR spectroscopy allowed the conclusion that the recognition process might involve H-bonding, electrostatic and pi-pi stacking interactions, the strength and the type of them depending oil the Substrate. The cooperative conjugation of the three types of interactions only occurs when terephthalate is the Substrate. Molecular dynamics Simulations (MD) in a periodic box of water solvent Molecules were also used to investigate the nature of the binding association between the receptor and the three aromatic dicarboxylate anions (phthalate, isophthalate, and terephthalate). These Studies confirmed that the (H6Me2[30]pbz(2)N(6))(6+) receptor encapsulates the terephthalate anion with the formation of all inclusion supermolecule stabilized by Multiple N-H center dot center dot center dot O hydrogen bonding and pi-pi interactions. The molecular recognition between the receptor and the other two aromatic anions, phthalate and isophthalate, also occurs via N-H center dot center dot center dot O hydrogen bonds, but outside of the macrocyclic cavity. The results are discussed in terms of energetic and entropic contributions and showed that the binding association between the receptor and these anions is favourable.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available