Formation of Two Dimensional Network Structure of DNA Molecules on Highly Ordered Pyrolytic Graphite Surface

2001 ◽  
Vol 40 (Part 1, No. 6A) ◽  
pp. 4217-4220 ◽  
Author(s):  
Shin-ichi Tanaka ◽  
Yasushi Maeda ◽  
Lin-Tao Cai ◽  
Hitoshi Tabata ◽  
Tomoji Kawai
2001 ◽  
Vol 40 (Part 2, No. 4B) ◽  
pp. L407-L409 ◽  
Author(s):  
Shin-ichi Tanaka ◽  
Lin-Tao Cai ◽  
Hitoshi Tabata ◽  
Tomoji Kawai

IUCrData ◽  
2019 ◽  
Vol 4 (1) ◽  
Author(s):  
Kai-Long Zhong ◽  
Guo-Qing Cao ◽  
Wei Song ◽  
Chao Ni

In the complex cation of the title salt, [Co(C12H8N2)3](C10H5O8)2·H2O, the CoII cation is situated on a twofold rotation axis and is coordinated in a distorted octahedral manner by six N atoms from three chelating 1,10-phenanthroline (phen) ligands. In the crystal, the non-coordinating 2,4,5-tricarboxybenzoate anions interact with each other via O—H...O hydrogen bonds, generating a two-dimensional network parallel to (100). Adjacent sheets are connected by waterO—H...Ocarboxylate hydrogen bonds, resulting in a three-dimensional network structure that surrounds the complex cations.


2009 ◽  
Vol 65 (3) ◽  
pp. m118-m120
Author(s):  
Olha Sereda ◽  
Helen Stoeckli-Evans

The title coordination polymer, [Cd3Co2(CN)12(C2H8N2)4]n, has an infinite two-dimensional network structure. The asymmetric unit is composed of two crystallographically independent CdIIatoms, one of which is located on a twofold rotation axis. There are two independent ethylenediamine (en) ligands, one of which bis-chelates to the Cd atom that sits in a general position, while the other bridges this Cd atom to that sitting on the twofold axis. The Cd atom located on the twofold rotation axis is linked to four equivalent CoIIIatomsviacyanide bridges, while the Cd atom that sits in a general position is connected to three equivalent CoIIIatomsviacyanide bridges. In this way, a series of trinuclear, tetranuclear and pentanuclear macrocycles are linked to form a two-dimensional network structure lying parallel to thebcplane. In the crystal structure, these two-dimensional networks are linkedviaN—H...N hydrogen bonds involving an en NH2H atom and a cyanide N atom, leading to the formation of a three-dimensional structure. This coordination polymer is only the second example involving a cyanometallate where the en ligand is present in both chelating and bridging coordination modes.


2006 ◽  
Vol 62 (4) ◽  
pp. m875-m877
Author(s):  
Wei-Bing Zhang ◽  
Shuang-Di Ruan ◽  
Shu-Juan Zhu ◽  
Hong-Ping Xiao ◽  
Sai-Ya Ye

In the title compound, [Cu2(C7H4O5S)2(C12H8N2)2(H2O)2]·3H2O, each copper(II) atom is coordinated by two N atoms from one 1,10-phenanthroline molecule, two carboxylate O atoms from two 2-sulfonatobenzoato dianions and one aqua O atom in a distorted square pyramidal geometry. The 2-sulfonatobenzoato dianions function as μ2-bridging ligands in the formation of a dinuclear complex. Intermolecular hydrogen-bond interactions link the dinuclear units into a two-dimensional network structure.


2006 ◽  
Vol 62 (7) ◽  
pp. o2965-o2966 ◽  
Author(s):  
Yan-Wen Lü ◽  
Bo-Hua Wang ◽  
Ge-Dong Cai ◽  
Zhen-Hua Li ◽  
Ping Wang

In the title compound, C15H11NO2, the benzene and phthalimide groups are planar and make a dihedral angle of 74.2 (1)° with one another. There are three weak C—H...O hydrogen bonds, forming a two-dimensional network structure.


2012 ◽  
Vol 68 (8) ◽  
pp. m1118-m1118
Author(s):  
Zhang Ping

In the title compound, [Cu(C13H7BrCl2NO)2], or CuL2{where HL= 2-[(E)-(2-chlorophenylimino)methyl]-6-bromo-4-chlorophenol}, the CuIIatom is located on an inversion center and has a square-planar coordination. In the crystal, complex molecules are linked via Cu...Cl interactions [2.9933 (11) Å], forming a two-dimensional network parallel to thebcplane. They are also Cl...Cl interactions [3.3709 (14) Å] present, which consolidate the two-dimensional network structure.


2015 ◽  
Vol 51 (41) ◽  
pp. 8664-8667 ◽  
Author(s):  
Lirong Xu ◽  
Lili Cao ◽  
Zongxia Guo ◽  
Zeqi Zha ◽  
Shengbin Lei

An imine-based 2D polymer side-functionalized with o-hydroxyl group was designed and synthesized on a highly oriented pyrolytic graphite surface.


2019 ◽  
Vol 75 (8) ◽  
pp. 1065-1072 ◽  
Author(s):  
Zhi-Chao Shao ◽  
Xiang-Ru Meng ◽  
Hong-Wei Hou

Aminobenzoic acid derivatives are widely used in the preparation of new coordination polymers since they contain O-atom donors, as well as N-atom donors, and have a rich variety of coordination modes which can lead to polymers with intriguing structures and interesting properties. Two new coordination polymers incorporating 1-aminobenzene-3,4,5-tricarboxylic acid (H3abtc), namely, poly[(μ3-1-amino-5-carboxybenzene-3,4-dicarboxylato)diaquacadmium(II)], [Cd(C9H5NO6)(H2O)2] n , (I), and poly[[bis(μ5-1-aminobenzene-3,4,5-tricarboxylato)triaquatrizinc(II)] dihydrate], {[Zn3(C9H4NO6)2(H2O)3]·2H2O} n , (II), have been prepared and structurally characterized by single-crystal X-ray diffraction. In polymer (I), each tridentate 1-amino-5-carboxybenzene-3,4-dicarboxylate (Habtc2−) ligand coordinates to three CdII ions to form a two-dimensional network structure, in which all of the CdII ions and Habtc2− ligands are equivalent, respectively. Polymer (II) also exhibits a two-dimensional network structure, in which three crystallographically independent ZnII ions are bridged by two crystallographically independent pentadentate 1-aminobenzene-3,4,5-tricarboxylate (abtc3−) ligands. This indicates that changing the metal ion can influence the coordination mode of the H3abtc-derived ligand and further influence the detailed architecture of the polymer. Moreover, the IR spectra, thermogravimetric analyses and fluorescence properties were investigated.


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