A Novel Hybrid Supramolecular Network Assembled from Perfect ??? Stacking of an Anionic Inorganic Layer and a Cationic Hydronium-Ion-Mediated Organic Layer

2004 ◽  
Vol 2004 (21) ◽  
pp. 4253-4258 ◽  
Author(s):  
Tzuoo-Tsair Luo ◽  
Yen-Hsiang Liu ◽  
Hui-Lien Tsai ◽  
Chan-Cheng Su ◽  
Chuen-Her Ueng ◽  
...  
Author(s):  
Ondřej Kaman ◽  
Ľubomír Smrčok ◽  
Róbert Gyepes ◽  
David Havlíček

The triclinic structure of the title compound, C6H8N+·H2PO4−, with three symmetry-independent structural units (Z′ = 3), is formed of separate organic and inorganic layers alternating along thebaxis. The building blocks of the inorganic layer are deformed H2PO4tetrahedra assembled into infinite ladders by short and hence strong hydrogen bonds. The anilinium cations forming the organic layer are not hydrogen bonded to one another, but they are anchored by four N—H...O crosslinks between the dihydrogen phosphate chains of adjacent ladders. Two H atoms of each –NH3group then form one normal and one bifurcated N—H...O hydrogen bond to the P=O oxygens of two tetrahedra of one chain, while the third H atom is hydrogen bonded to the nearest O atom of an adjacent chain belonging to another dihydrogen phosphate ladder.


2013 ◽  
Vol 68 (4) ◽  
pp. 403-407 ◽  
Author(s):  
Ting-Ting Kang ◽  
Hao Tang ◽  
Yong-Li Wei ◽  
Shuang-Quan Zang

A chiral two-dimensional (2D) coordination polymer {[Zn(cmmb)(1,4-bbi)]·H2O}n (1) has been synthesized by a hydrothermal reaction of Zn(NO3)2·6H2O with 4- (carboxymethoxy)-2-methylbenzoic acid (H2cmmb) and 1,1`-(1,4-butanediyl)bis(imidazole) (1,4-bbi). It has been characterized by elemental analysis, X-ray crystallography, IR spectroscopy and thermogravimetry, and also by its fluorescence properties. The metal-organic layer of the complex is held together with its neighbors via C-H···O hydrogen bonds to give rise to a chiral three-dimensional supramolecular network.


2015 ◽  
Vol 1 (8) ◽  
pp. e1500330 ◽  
Author(s):  
Xiaoyan Wu ◽  
Shifeng Jin ◽  
Zhizhen Zhang ◽  
Liwei Jiang ◽  
Linqin Mu ◽  
...  

Organic carbonyl compounds represent a promising class of electrode materials for secondary batteries; however, the storage mechanism still remains unclear. We take Na2C6H2O4 as an example to unravel the mechanism. It consists of alternating Na-O octahedral inorganic layer and π-stacked benzene organic layer in spatial separation, delivering a high reversible capacity and first coulombic efficiency. The experiment and calculation results reveal that the Na-O inorganic layer provides both Na+ ion transport pathway and storage site, whereas the benzene organic layer provides electron transport pathway and redox center. Our contribution provides a brand-new insight in understanding the storage mechanism in inorganic-organic layered host and opens up a new exciting direction for designing new materials for secondary batteries.


1963 ◽  
Vol 44 (1) ◽  
pp. 47-66 ◽  
Author(s):  
W. Nocke ◽  
H. Breuer

ABSTRACT A method for the chemical determination of 16-epi-oestriol in the urine of nonpregnant women with a qualitative sensitivity of less than 0.5 μg/24 h is described. The separation of 16-epi-oestriol and oestriol is accomplished by converting 16-epi-oestriol into its acetonide, a reaction which is stereoselective for cis-glycols and therefore not undergone by oestriol as a trans-glycol. Following partition between chloroform and aqueous alkali, the acetonide of 16-epi-oestriol is completely separated with the organic layer whereas oestriol as a strong phenol remains in the alkaline phase. 16-epi-oestriol is chromatographed on alumina as the acetonide and determined as a Kober chromogen. This procedure can easily be incorporated into the method of Brown et al. (1957 b) thus making possible the simultaneous routine assay of oestradiol-17β, oestrone, oestriol and 16-epi-oestriol from one sample of urine. The specificity of the method was established by separation of 16-epi-oestriol from nonpregnancy urine as the acetonide, hydrolysis of the acetonide by phosphoric acid, isolation of the free compound by microsublimation and identification by micro melting point, colour reactions and chromatography. The accuracy of the method is given by a mean recovery of 64% for pure crystalline 16-epi-oestriol when added to hydrolysed urine in 5–10 μg amounts. The precision is given by s = 0.24 μg/24 h. For the duplicate determination of 16-epi-oestriol the qualitative sensitivity is 0.44 μg/24 h, the maximum percentage error being ± 100% The quantitative sensitivity (±25% error) is 1.7 μg/24 h.


2021 ◽  
Vol 143 (5) ◽  
pp. 2194-2199 ◽  
Author(s):  
Geoffrey T. Nash ◽  
Taokun Luo ◽  
Guangxu Lan ◽  
Kaiyuan Ni ◽  
Michael Kaufmann ◽  
...  

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Marco Diers ◽  
Robert Weigel ◽  
Heike Culmsee ◽  
Christoph Leuschner

Abstract Background Organic carbon stored in forest soils (SOC) represents an important element of the global C cycle. It is thought that the C storage capacity of the stable pool can be enhanced by increasing forest productivity, but empirical evidence in support of this assumption from forests differing in tree species and productivity, while stocking on similar substrate, is scarce. Methods We determined the stocks of SOC and macro-nutrients (nitrogen, phosphorus, calcium, potassium and magnesium) in nine paired European beech/Scots pine stands on similar Pleistocene sandy substrates across a precipitation gradient (560–820 mm∙yr− 1) in northern Germany and explored the influence of tree species, forest history, climate, and soil pH on SOC and nutrient pools. Results While the organic layer stored on average about 80% more C under pine than beech, the pools of SOC and total N in the total profile (organic layer plus mineral soil measured to 60 cm and extrapolated to 100 cm) were greater under pine by about 40% and 20%, respectively. This contrasts with a higher annual production of foliar litter and a much higher fine root biomass in beech stands, indicating that soil C sequestration is unrelated to the production of leaf litter and fine roots in these stands on Pleistocene sandy soils. The pools of available P and basic cations tended to be higher under beech. Neither precipitation nor temperature influenced the SOC pool, whereas tree species was a key driver. An extended data set (which included additional pine stands established more recently on former agricultural soil) revealed that, besides tree species identity, forest continuity is an important factor determining the SOC and nutrient pools of these stands. Conclusion We conclude that tree species identity can exert a considerable influence on the stocks of SOC and macronutrients, which may be unrelated to productivity but closely linked to species-specific forest management histories, thus masking weaker climate and soil chemistry effects on pool sizes.


2021 ◽  
Author(s):  
Ruoru Yang ◽  
Bonan Li ◽  
Xiaoyong Lai ◽  
Xiaojing Yu ◽  
Boxin Xiao ◽  
...  

A novel irregular-octagonal-prism-shaped host–guest supramolecular network was synthesized and showed excellent photocatalytic splitting of water performance.


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