Self-Assembly of Dialkyltin Moieties and Mercaptobenzoic Acid into Macrocyclic Complexes with Hydrophobic “Pseudo-Cage” or Double-Cavity Structures: Supramolecular Infrastructures Involving Intermolecular CH⋅⋅⋅S Weak Hydrogen Bonds and π–π Interactions

2006 ◽  
Vol 12 (2) ◽  
pp. 420-428 ◽  
Author(s):  
Chunlin Ma ◽  
Qingfu Zhang ◽  
Rufen Zhang ◽  
Daqi Wang
2010 ◽  
Vol 65 (2) ◽  
pp. 152-156
Author(s):  
Di Sun ◽  
Cheng-Feng Yang ◽  
Zhan-Hua Wei ◽  
Geng-Geng Luo ◽  
Na Zhang ◽  
...  

A new three-dimensional (3D) supramolecular framework, [Ag2(bipy)2(bdc)·4H2O]n 1, has been synthesized by the ultrasonic reaction of Ag2O, bipy and H2bdc (H2bdc = 1,4-benzenedicarboxylic acid; bipy = 4,4’-bipyridine) at room temperature. It exhibits a new 3D supramolecular framework which is built from cationic Ag-bipy chains and anionic bdc-H2O sheets through hydrogen bonds, π · · ·π stacking and C-H· · ·π interactions. Additionally, the photoluminescent and thermal properties of 1 were investigated.


2011 ◽  
Vol 66 (1) ◽  
pp. 83-87

The X-ray crystal structures of the three compounds N,N’-dibenzylterephthalamide, 1, N,N’-dibenzyl- N,N’-dimethylterephthalamide, 2, and N,N,N’ ,N’-tetrabenzylterephthalamide, 3, were determined. Compound 1 fits into the general pattern of disubstituted terephthalamides, with crystallographic inversion symmetry and classical hydrogen bonds linking the molecules into chains parallel to the short axis. Compound 2 also displays inversion symmetry, but the packing only involves two weak hydrogen bonds of the form C-Hmethyl ・ ・ ・ O. The complex packing of compound 3, which possesses no crystallographic symmetry, involves only two C-H・ ・ ・O contacts; these are augmented by three C-H・ ・ ・π interactions


Author(s):  
Nutchanikan Phiromphu ◽  
Kittipong Chainok ◽  
Apisit Songsasen ◽  
Tanwawan Duangthongyou

In the title hydrated azo dye, C10H10N4OS·H2O, the benzene and thiazole, are nearly coplanar, with a dihedral angle between their mean planes of 4.69 (17)°. The aromatic rings on the –N=N– moiety exhibit a trans configuration. The crystal structure features many types of intermolecular interactions involving all the functional groups – strong hydrogen bonds (N...H and O...H), weak hydrogen bonds (C—H...O and C—H...N), C—H...π and π–π interactions – resulting in the formation of a three-dimensional framework.


2014 ◽  
Vol 70 (a1) ◽  
pp. C638-C638
Author(s):  
Aouaouche Benkanoun ◽  
Fadéla Balegroune ◽  
Achoura Guehria-Laidoudi ◽  
Slimane Dahaoui ◽  
Claude Lecomte

The main strategy for preparing novel multifunctional materials is based on self-assembly method which employs polydentate organic ligands containing N- or O-donor as building blocks. In this context, those ligands like imidazole or carboxylate groups are of special interest due to their good coordination ability and diverse coordination modes [1]. As a part of our investigations of extended structures with mixed ligands, new complexes [Co(Hipht)2(Im)2(H2O)2] and [Co(Tpht)(Im)3(H2O)2].H2O were obtained by direct method, then characterized by IR spectroscopy, TG/ATD and X-ray crystallography. In the compound [Co(Hipht)2(Im)2(H2O)2], CoII is located on a symmetry center, surrounded by two aqua ligands, two hydrogeno-isophthalate ligands and two imidazole molecules, where all ligands adopt monodentate mode. The complex's geometry consist of two intermolecular N-H...O bonds (2,157 Å and 2,630 Å) formed by one H atom of imidazole ligand and oxygen atoms of acid molecules evolving along two directions, giving rise to R24 (16) synthons. The interplanar distance of 3,718 Å between two parallel imidazole rings reveals the existence of Π-Π interactions. In the [Co(Tpht)(Im)3(H2O)2].H2O [2], the Co cation exhibits an octahedral coordination sphere, with two aqua, three N-coordinated imidazole ligands and one terephthalato dianion. The three independent imidazole groups and the single terephtalate dianion, all unidentate participate respectively as donor and acceptor in strong to moderate hydrogen bonds, and allow the recognition of supramolecular dimensionality. The backbone of the architecture is the helical hydrogen-bonded ladder running along b axis, composed of alternating R44(10) and R33(8) heterosynthons, which are developed in bicyclic sheets. Non covalent interactions play a significant role in this class of materials [3], in fact, extended hydrogen bonds networks associated to Π-Π interactions lead to 3D supramolecular architecture for the two complexes.


2014 ◽  
Vol 67 (10) ◽  
pp. 1504
Author(s):  
Zhu-Yan Zhang ◽  
Zhao-Peng Deng ◽  
Li-Hua Huo ◽  
Shu-E Zhang ◽  
Hui Zhao ◽  
...  

Self-assembly of three flexible bis(pyridyl) molecules with different inorganic acids (HPF6, HClO4, and HNO3) leads to the formation of eight salts, which exhibit diverse architectures involving hydrogen bonding and anion–π interactions. The three types of inorganic anions in these salts formed anion–π interactions with HM+ and H2M2+ except for 2, in which the six F atoms were involved in hydrogen bonds. Anion–π interactions produced diverse motifs of one (anion)-to-one (cation) in 1, 3, 4, and 6, two (anion)-to-one (cation) in 5 and 7, and (4,4) layer in 8. Hydrogen bonds resulted in interesting supramolecular architectures, such as right- and left-handed helical chains in 3, 2-fold interpenetrating networks in 5, and 3-fold interpenetrating networks in 8. Structural analyses indicated that the conformations of the three flexible asymmetrical bis(pyridyl) molecules and the non-covalent bonding interactions, such as hydrogen bonds and anion···π interactions, play crucial roles in the final architectures of these salts. Thermogravimetric analyses indicated that the thermal stability of the eight salts decreased in the order of perchlorates, hexafluorophosphates, and nitrates. The emission intensity of the perchlorates is much stronger than that of the hexafluorophosphates, nitrates, and their corresponding organic molecules in the solid state at room temperature.


2021 ◽  
Author(s):  
Jian Su ◽  
Shuai Yuan ◽  
Yi-Xun Cheng ◽  
Zhi-Mei Yang ◽  
Jing-Lin Zuo

Controlled synthesis of hydrogen-bonded organic frameworks (HOFs) remains challenging, because the self-assembly of ligands is not only directed by weak hydrogen bonds, but also affected by other competing van der...


RSC Advances ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 6002-6007
Author(s):  
Clément Drou ◽  
Théo Merland ◽  
Antoine Busseau ◽  
Sylvie Dabos-Seignon ◽  
Antoine Goujon ◽  
...  

New penta(organo)fullerene bearing five benzo[ghi]perylenetriimide units has been synthesized to form self-assemblies through π–π interactions.


2014 ◽  
Vol 70 (6) ◽  
pp. o679-o679 ◽  
Author(s):  
Hakima Chicha ◽  
El Mostapha Rakib ◽  
Abdellah Hannioui ◽  
Mohamed Saadi ◽  
Lahcen El Ammari

The indazole ring system of the title compound, C17H18ClN3O4S, is almost planar (r.m.s. deviation = 0.0113 Å) and forms dihedral angles of 32.22 (8) and 57.5 (3)° with the benzene ring and the mean plane through the 4-ethoxy group, respectively. In the crystal, molecules are connected by pairs of N—H...O hydrogen bonds into inversion dimers, which are further linked by π–π interactions between the diazole rings [intercentroid distance = 3.4946 (11) Å], forming chains parallel to [101].


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