scholarly journals 'Metalloaromaticity' of metal chelate ring. π–π stacking interactions in solid-state supramolecular architecture of copper(II) complexes with aromatic ligands

2004 ◽  
Vol 60 (a1) ◽  
pp. s304-s304 ◽  
Author(s):  
V. Kravtsov
Keyword(s):  
Solid State ◽  
Chelate Ring ◽  
Metal Chelate ◽  
Stacking Interactions ◽  
Supramolecular Architecture ◽  
Π Stacking

X-ray Crystal Structure of Gallium Tris- (8-hydroxyquinoline):  Intermolecular π−π Stacking Interactions in the Solid State

1999 ◽  
Vol 11 (3) ◽  
pp. 530-532 ◽  
Author(s):  
Yue Wang ◽  
Weixing Zhang ◽  
Yanqin Li ◽  
Ling Ye ◽  
Guangdi Yang
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Stacking Interactions ◽  
X Ray ◽  
Π Stacking

scholarly journals Bis(thiocyanato-κN)[tris(pyridin-2-ylmethyl)amine-κ4N]iron(II)

2014 ◽  
Vol 70 (2) ◽  
pp. m35-m35
Author(s):  
Jing-Wei Dai ◽  
Zhao-Yang Li ◽  
Osamu Sato
Keyword(s):  
Hydrogen Bonds ◽  
Octahedral Geometry ◽  
Title Complex ◽  
Stacking Interactions ◽  
Supramolecular Architecture ◽  
Two Dimensional ◽  
Π Stacking ◽  
Centroid Distance ◽  
Solvent Molecules ◽  
Amine Ligand

In the title complex, [Fe(NCS)2(C18H18N4)], the FeIIcation is chelated by a tris(2-pyridylmethyl)amine ligand and coordinated by two thiocyanate anions in a distorted N6octahedral geometry. In the crystal, weak C—H...S hydrogen bonds and π–π stacking interactions between parallel pyridine rings of adjacent molecules [centroid–centroid distance = 3.653 (3) Å] link the molecules into a two-dimensional supramolecular architecture. The structure contains voids of 124 (9) Å3, which are free of solvent molecules.

Pentafluorophenyl Copper–Pyridine Complexes: Synthesis, Supramolecular Structures via Cuprophilic and π-Stacking Interactions, and Solid-State Luminescence

2011 ◽  
Vol 31 (4) ◽  
pp. 1546-1558 ◽  
Author(s):  
Ami Doshi ◽  
Anand Sundararaman ◽  
Krishnan Venkatasubbaiah ◽  
Lev N. Zakharov ◽  
Arnold L. Rheingold ◽  
...  
Keyword(s):  
Solid State ◽  
Supramolecular Structures ◽  
Stacking Interactions ◽  
Pyridine Complexes ◽  
Π Stacking ◽  
State Luminescence

Suppressing π–π stacking interactions for enhanced solid-state emission of flat aromatic molecules via edge functionalization with picket-fence-type groups

2020 ◽  
Vol 8 (48) ◽  
pp. 17289-17296
Author(s):  
Hye Jin Cho ◽  
Sang Won Kim ◽  
Sungjin Kim ◽  
Sangback Lee ◽  
Juhyen Lee ◽  
...  
Keyword(s):  
Solid State ◽  
Light Emitting Diodes ◽  
Organic Light Emitting Diodes ◽  
Stacking Interactions ◽  
Light Emitting ◽  
Aromatic Molecules ◽  
Organic Light ◽  
Π Stacking ◽  
Picket Fence ◽  
Π Stacking Interaction

Picket-fence-type substituents effectively suppress the π–π stacking interaction of flat aromatic molecules and enhance solid-state emission for application in organic light-emitting diodes.

Assembly of Three Cadmium(II) Complexes Based on Flexible α,ѡ-Bis(benzimidazolyl)alkane Ligands

2012 ◽  
Vol 67 (8) ◽  
pp. 791-798 ◽  
Author(s):  
Jian-Chen Geng ◽  
Cui-Huan Jiao ◽  
Jin-Ming Hao ◽  
Guang-Hua Cui
Keyword(s):  
Solid State ◽  
Chain Structure ◽  
Helical Chain ◽  
Supramolecular Network ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Π Stacking ◽  
Elemental Analyses ◽  
Network Complex

Three flexible α,ѡ-bis(5,6-dimethylbenzimidazolyl)alkane ligands with different spacers were reacted with CdX2 (X = Cl, Br, I) hydrothermally, resulting in three coordination architectures, namely [CdI2(L1)]n (1), [CdBr2(L2)]n (2), and Cd2Cl4(L3)2 (3) [L1 = 1,3-bis(5,6- dimethylbenzimidazole)propane, L2 = 1,5-bis(5,6-dimethylbenzimidazole)pentane, L3 = 1,6- bis(5,6-dimethylbenzimidazole)hexane]. They have been characterized by elemental analyses, IR spectra, thermogravimetric (TG) analysis, and single-crystal X-ray diffraction. Complex 1displays a helical chain linked by the ligands L1, and a 2D supramolecular network is constructed through π-π stacking interactions; complex 2shows a helical chain structure with connections through two kinds of strong π-π stacking interactions into an intricate 3D supramolecular network; complex 3 contains dinuclear metallomacrocycles. The fluorescence properties of 1-3have been investigated in the solid state

Synthesis and crystal structure of a novel prochiral ketoimine: (E)-acetophenoneO-diphenylphosphoryl oxime

2015 ◽  
Vol 71 (3) ◽  
pp. 181-184
Author(s):  
Sean H. Majer ◽  
Joseph M. Tanski
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Stacking Interactions ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
Face To Face ◽  
Π Stacking

A novel activated prochiral ketoimine, (E)-acetophenoneO-diphenylphosphoryl oxime, C20H18NO2P, with an electron-withdrawing substituent on the imine N atom similar to other prochiral ketoimines, has been synthesized and the X-ray crystal stucture determined. The molecules pack together in the solid stateviaweak intermolecular C—H...O interactions and both face-to-face and edge-to-face π-stacking interactions.

scholarly journals The role of π–π stacking and hydrogen-bonding interactions in the assembly of a series of isostructural group IIB coordination compounds

2019 ◽  
Vol 75 (2) ◽  
pp. 178-188 ◽  
Author(s):  
Taraneh Hajiashrafi ◽  
Roghayeh Zekriazadeh ◽  
Keith J. Flanagan ◽  
Farnoush Kia ◽  
Antonio Bauzá ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Solid State ◽  
Coordination Compounds ◽  
Spectroscopic Techniques ◽  
Stacking Interactions ◽  
X Ray Crystallography ◽  
Hydrogen Bonding Interactions ◽  
Π Stacking ◽  
Research Domain

The supramolecular chemistry of coordination compounds has become an important research domain of modern inorganic chemistry. Herein, six isostructural group IIB coordination compounds containing a 2-{[(2-methoxyphenyl)imino]methyl}phenol ligand, namely dichloridobis(2-{(E)-[(2-methoxyphenyl)azaniumylidene]methyl}phenolato-κO)zinc(II), [ZnCl2(C28H26N2O4)], 1, diiodidobis(2-{(E)-[(2-methoxyphenyl)azaniumylidene]methyl}phenolato-κO)zinc(II), [ZnI2(C28H26N2O4)], 2, dibromidobis(2-{(E)-[(2-methoxyphenyl)azaniumylidene]methyl}phenolato-κO)cadmium(II), [CdBr2(C28H26N2O4)], 3, diiodidobis(2-{(E)-[(2-methoxyphenyl)azaniumylidene]methyl}phenolato-κO)cadmium(II), [CdI2(C28H26N2O4)], 4, dichloridobis(2-{(E)-[(2-methoxyphenyl)azaniumylidene]methyl}phenolato-κO)mercury(II), [HgCl2(C28H26N2O4)], 5, and diiodidobis(2-{(E)-[(2-methoxyphenyl)azaniumylidene]methyl}phenolato-κO)mercury(II), [HgI2(C28H26N2O4)], 6, were synthesized and characterized by X-ray crystallography and spectroscopic techniques. All six compounds exhibit an infinite one-dimensional ladder in the solid state governed by the formation of hydrogen-bonding and π–π stacking interactions. The crystal structures of these compounds were studied using geometrical and Hirshfeld surface analyses. They have also been studied using M06-2X/def2-TZVP calculations and Bader's theory of `atoms in molecules'. The energies associated with the interactions, including the contribution of the different forces, have been evaluated. In general, the π–π stacking interactions are stronger than those reported for conventional π–π complexes, which is attributed to the influence of the metal coordination, which is stronger for Zn than either Cd or Hg. The results reported herein might be useful for understanding the solid-state architecture of metal-containing materials that contain M II X 2 subunits and aromatic organic ligands.

Hydrogen-bridged chelate ring-assisted π-stacking interactions

2012 ◽  
Vol 68 (1) ◽  
pp. 71-79 ◽  
Author(s):  
Hasan Karabıyık ◽  
Hande Karabıyık ◽  
Nazan Ocak İskeleli
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bond ◽  
Intramolecular Hydrogen Bond ◽  
Tautomeric Form ◽  
Chelate Ring ◽  
Molecular Crystals ◽  
Stacking Interactions ◽  
Aromatic Rings ◽  
Π Stacking ◽  
Intramolecular Hydrogen

A salicylideneaniline (SA) derivative, (6Z)-6-({[2-(hydroxymethyl)phenyl]amino}methylidene)-3,5-dimethoxycyclohexa-2,4-dien-1-one monohydrate, has an increased aromaticity within its hydrogen-bridged chelate ring owing to its NH character. In the reported crystal structure, nonconventional π-stacking interactions, which are referred to as hybrid π-stacking interactions, are observed between a quasiaromatic chelate ring, formed as a result of the resonance-assisted intramolecular hydrogen bond and ordinary aromatic rings. Besides, π-stacking interactions are also seen between two hydrogen-bridged quasiaromatic chelate rings, which are referred to as pure π-stacking interactions. A CSD search has revealed that both kinds of interactions are frequently observed in molecular crystals of SA derivatives in fully or partially NH tautomeric form, and aromaticity levels of certain fragments of SA derivatives have dramatic effects on their stacking arrangements. These interactions are distinguished from the usual π...π interactions by their formation character, i.e. both σ- and π-deficient and σ-deficient character of pure interactions is more pronounced than that of the hybrid ones.

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