Two temperature-dependent Cd(II)-based coordination polymers with mixed adenine nucleobase and benzene-1,4-dicarboxylic acid: synthesis, structures and fluorescence properties

2020 ◽  
Vol 73 (9) ◽  
pp. 1490-1501 ◽  
Author(s):  
Hong-Kun Zhao ◽  
Han-Wen Yang ◽  
Bo Ding ◽  
Xiu-Guang Wang ◽  
Xian-Chen Meng ◽  
...  
Keyword(s):  
Dicarboxylic Acid ◽  
Coordination Polymers ◽  
Acid Synthesis ◽  
Fluorescence Properties ◽  
Temperature Dependent ◽  
Two Temperature

Assembly of two novel coordination polymers by selecting ditopic or chelating auxiliary ligands with naphthalene-2,6-dicarboxylic acid: synthesis, structure and luminescence sensing

2020 ◽  
Vol 76 (12) ◽  
pp. 1076-1084
Author(s):  
Yuxiang Zuo ◽  
Jie Yang ◽  
Cheng Chen ◽  
Yun-Shan Xue ◽  
Jun Zhang
Keyword(s):  
Dicarboxylic Acid ◽  
Coordination Polymers ◽  
Chemical Sensors ◽  
Acid Synthesis ◽  
Selective Detection ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Biochemical Processes ◽  
Solvothermal Methods

The FeIII ion as a ubiquitous metal plays a key role in biochemical processes. Iron deficiency or excess in the human body can induce various diseases. Thus, effective detection of the FeIII ion has been deemed an issue of focus. To develop more crystalline chemical sensors for the selective detection of Fe3+, two novel two-dimensional (2D) coordination polymers, namely, poly[[[μ-bis(pyridin-4-yl)amine-κ2 N:N′](μ-naphthalene-2,6-dicarboxylato-κ2 O 2:O 6)zinc(II)] 0.5-hydrate], {[Zn(C12H6O4)(C10H9N3)]·0.5H2O} n , 1, and poly[(4,4′-dimethyl-2,2′-bipyridine-κ2 N,N′)(μ-naphthalene-2,6-dicarboxylato-κ2 O 2:O 6)hemi(μ-naphthalene-2,6-dicarboxylic acid-κ2 O 2:O 6)copper(II)] [Cu(C12H6O4)(C12H12N2)(C12H8O4)0.5] n , 2, have been prepared using solvothermal methods. Single-crystal X-ray diffraction analysis shows that compound 1 is an undulating twofold interpenetrated 2D (4,4)-sql network and compound 2 is a twofold interpenetrated 2D honeycomb-type network with a (6,3)-hcb topology. In addition, 1 exhibits highly selective sensing for the Fe3+ ion.

From 1D to 3D lanthanide coordination polymers constructed with pyridine-3,5-dicarboxylic acid: synthesis, crystal structures, and catalytic properties

RSC Advances ◽  
2016 ◽  
Vol 6 (68) ◽  
pp. 63425-63432 ◽  
Author(s):  
Xiao-Ming Lin ◽  
Ji-Liang Niu ◽  
Pei-Xian Wen ◽  
Yan-Na Lu ◽  
Lei Hu ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Dicarboxylic Acid ◽  
Crystal Structures ◽  
Coordination Polymers ◽  
Catalytic Properties ◽  
Structural Difference ◽  
Acid Synthesis ◽  
Lanthanide Coordination Polymers ◽  
Lanthanide Contraction

Three series of lanthanide coordination polymers have been synthesized. The structural difference may be derived from the lanthanide contraction. Moreover, we also discussed the size-selective catalytic activity towards cyanosilylation of aldehydes.

scholarly journals Thermochromic aggregation-induced dual phosphorescence via temperature-dependent sp3-linked donor-acceptor electronic coupling

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Tao Wang ◽  
Zhubin Hu ◽  
Xiancheng Nie ◽  
Linkun Huang ◽  
Miao Hui ◽  
...  
Keyword(s):  
Excited State ◽  
Room Temperature ◽  
Electronic Coupling ◽  
Temperature Dependent ◽  
Molecular Systems ◽  
Donor And Acceptor ◽  
Theoretical Investigations ◽  
Donor Acceptor ◽  
And Control ◽  
Two Temperature

AbstractAggregation-induced emission (AIE) has proven to be a viable strategy to achieve highly efficient room temperature phosphorescence (RTP) in bulk by restricting molecular motions. Here, we show that by utilizing triphenylamine (TPA) as an electronic donor that connects to an acceptor via an sp3 linker, six TPA-based AIE-active RTP luminophores were obtained. Distinct dual phosphorescence bands emitting from largely localized donor and acceptor triplet emitting states could be recorded at lowered temperatures; at room temperature, only a merged RTP band is present. Theoretical investigations reveal that the two temperature-dependent phosphorescence bands both originate from local/global minima from the lowest triplet excited state (T1). The reported molecular construct serves as an intermediary case between a fully conjugated donor-acceptor system and a donor/acceptor binary mix, which may provide important clues on the design and control of high-freedom molecular systems with complex excited-state dynamics.

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