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Cited by 33 publications
(14 citation statements)
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“…A variety of studies have demonstrated the coordination nanostructures by altering organic ligands, such as carboxylate, 3,5,12,18 hydroxyl, 14,20,21 pyridine, 9,22-25 and triazine. [26][27][28][29][30] The triazine derivatives are important in a range of areas as ligands for supramolecular self-assembly of more complex mixed layers, hence it may be interesting to study the coordination properties of the triazine derivatives.…”
Section: Introductionmentioning
confidence: 99%
“…A variety of studies have demonstrated the coordination nanostructures by altering organic ligands, such as carboxylate, 3,5,12,18 hydroxyl, 14,20,21 pyridine, 9,22-25 and triazine. [26][27][28][29][30] The triazine derivatives are important in a range of areas as ligands for supramolecular self-assembly of more complex mixed layers, hence it may be interesting to study the coordination properties of the triazine derivatives.…”
Section: Introductionmentioning
confidence: 99%
“…12–14 Compounds containing NH protons, such as imidazoles, pyrazoles, amides, amino, thiourea, and urea derivatives, have been extensively used as chromogenic and fluorogenic sensors for anions, and naturally for F − anions. 1,2,13–25 This is due to the ability of the NH proton to participate in strong hydrogen-bonding interactions with F − . 16…”
Section: Introductionmentioning
confidence: 99%
“…Recognition of toxic anions has recently become a signicant aspect of supramolecular and coordination chemistry owing to its potential applications in environmental, biological, industrial, and agricultural elds. [1][2][3][4][5][6][7][8][9][10][11] In particular, uoride (F À ) sensing is attracting considerable attention because of the small size, high charge density, and hard Lewis characteristics of F À . Fluoride is used to treat osteoporosis and maintain dental health, and is readily absorbed by the human body but excreted sluggishly.…”
Section: Introductionmentioning
confidence: 99%
“…In artificial molecular receptors, a strong and selective binding of anions, such as chloride [11], carboxylates [12][13][14][15], and phosphates [16,17], might be realized by the selection of a proper molecular platform and decorating it with neutral (thio)amide [18][19][20], (thio)urea [19][20][21][22], pyrrole [23,24], and/or cationic ammonium [25], guanidinium [14,26], and imidazolium [27,28] binding groups. Despite enormous progress in the field of anion supramolecular chemistry in recent decades [1,2,19,[29][30][31], the prediction of exact anion affinity and selectivity of a designed receptor is still a challenging task due to difficulties in simulating the correct contribution of solvation and entropy effects on the stability of the supramolecular receptor-anion complex [9,[32][33][34][35][36][37]. This is particularly relevant for the Materials 2022, 15, 692 2 of 15 more demanding chiral anion recognition, as the differences in Gibbs free energy between diastereomeric complexes are usually expected not to exceed 2 kcal•mol −1 .…”
Section: Introductionmentioning
confidence: 99%