Formation of a 1D-polymeric chain of Hg building blocks through C–C coupling under ambient conditions

2013 ◽  
Vol 42 (30) ◽  
pp. 10687 ◽  
Author(s):  
Shaikh M. Mobin ◽  
Veenu Mishra ◽  
Priti Ram ◽  
Anil Birla ◽  
Pradeep Mathur
2021 ◽  
Author(s):  
Safaa Eldin H. Etaiw ◽  
Safaa N. Abdou Nabih Abdou

Abstract A new 3D-host-guest supramolecular coordination polymer (SCP); ∞3[(Cu3(CN)3)2.(DAHP)], 1 [1,7-diaminoheptane=.(DAHP)] had been synthesized by self-assembly at ambient conditions. X-ray single crystal diffraction of SCP 1 indicated the formation of two-fold [Cu3(CN)3]2 units containing tetrahedral copper(I) atoms which are arranged in unique way to create 3D-network. The neutral [Cu3(CN)3]2 building blocks create unique complex structure containing the minicycle [Cu2(μ3-CN)2] motif with wide cavities enable to capsulate the long chain DAHP as guest molecule. The topology of 1 had been studied by elemental analysis, IR-spectra and thermogravimetric analyses. The topology of 1 had been compared with the prototype SCP containing different aliphatic diamines which indicated the effect of structural variability and flexibility of aliphatic diamines on the network structure of these SCP. The catalytic and photo-catalytic activity of 1 was studied for mineralization of methylene blue (MB) utilizing H2O2 as an oxidant.


2019 ◽  
Vol 15 ◽  
pp. 2930-2935
Author(s):  
Daniel P Pienaar ◽  
Kamogelo R Butsi ◽  
Amanda L Rousseau ◽  
Dean Brady

The acylation of the acetonitrile anion with lactones and esters in ethereal solvents was successfully exploited using inexpensive KOt-Bu to obtain a variety of β-ketonitriles and trifunctionalized building blocks, including useful O-unprotected diols. It was discovered that lactones react to produce the corresponding derivatized cyclic hemiketals. Furthermore, the addition of a catalytic amount of isopropanol, or 18-crown-6, was necessary to facilitate the reaction and to reduce side-product formation under ambient conditions.


Author(s):  
Kunal S. Mali ◽  
Steven De Feyter

Self-assembled physisorbed monolayers consist of regular two-dimensional arrays of molecules. Two-dimensional self-assembly of organic and metal–organic building blocks is a widely used strategy for nanoscale functionalization of surfaces. These supramolecular nanostructures are typically sustained by weak non-covalent forces such as van der Waals, electrostatic, metal–ligand, dipole–dipole and hydrogen bonding interactions. A wide variety of structurally very diverse monolayers have been fabricated under ambient conditions at the liquid–solid and air–solid interface or under ultra-high-vacuum (UHV) conditions at the UHV–solid interface. The outcome of the molecular self-assembly process depends on a variety of factors such as the nature of functional groups present on assembling molecules, the type of solvent, the temperature at which the molecules assemble and the concentration of the building blocks. The objective of this review is to provide a brief account of the progress in understanding various parameters affecting two-dimensional molecular self-assembly through illustration of some key examples from contemporary literature.


Author(s):  
Annika Schmidt ◽  
Anna Krupp ◽  
Eva Rebecca Barth ◽  
Carsten Strohmann

The title compounds, C10H16O2Si (1) and C17H18OSi (2), are classified as dihydrofurylsilanes, which show great potential as building blocks for various functionalized silanes. They both crystallize in the space group P\overline{1} in the triclinic crystal system. Analyses of the Hirshfeld surfaces show packing-determining interactions for both compounds, resulting in a polymeric chain along the [011] for silane 1 and a layered-interconnected structure along the b-axis direction for silane 2.


2021 ◽  
Vol 9 ◽  
Author(s):  
Sijia Miao ◽  
Yuljae Cho

Colloidal quantum dots (CQDs) have attracted tremendous research interests in future-generation energy, electronic, optoelectronic, and bio-imaging applications due to their fascinating material properties, such as solution processability at room temperature and under ambient conditions, compatibility with various functional materials, and high photostability as well as photosensitivity. Among the various optoelectronic applications of CQDs, optical light sensors, which convert photonic energy into electrical signals, have been of particular interest because they are one of the key building blocks for modern communication and imaging applications, including medical X-ray and near-infrared imaging, visible light cameras, and machine vision. However, CQDs, which have been widely researched for photodetectors (PDs) so far, contain toxic and hazardous heavy metals, namely, lead (Pb), cadmium (Cd), and mercury (Hg). These substances are extremely toxic and harmful to the environment as well as human beings. Therefore, it is highly desirable to substitute CQDs containing heavy metals with nontoxic and environmentally friendly ones to realize green optoelectronics. In this review article, we introduce various kinds of heavy metal–free CQDs and their PD applications. This article comprehensively includes working mechanisms of PDs, various kinds of nontoxic and environmentally friendly CQD-based PDs, advanced heterojunction PDs, and discussion for future perspectives.


2015 ◽  
Vol 6 (36) ◽  
pp. 6579-6584 ◽  
Author(s):  
Yu Xiong ◽  
Xiaolan Qiao ◽  
Hongxiang Li

Conjugated polymers containing nitrile-substituted thienyl and phenyl units displayed high electron mobility under ambient conditions.


1996 ◽  
Vol 52 (6) ◽  
pp. 966-975 ◽  
Author(s):  
C.-R. Lee ◽  
C.-C. Wang ◽  
Y. Wang

This work illustrates the structural relationship between three types of metal squarates as well as the ligand in its acid form and in its monoanion salt. Squaric acid, H2C4O4, is known to have a polymeric layer structure with planar molecules connected through intermolecular hydrogen bonds. The interlayer distance is only 2.649 Å. The crystal of H2NMe2[H3(C4O4)2] is found to contain columns of [H3(C4O4)2 −] repeating units, again connected by intermolecular hydrogen bonds. Within the repeated unit, there is a symmetric hydrogen bond connected to two HC4O4 moieties. A new type of metal squarate with M(HC4O4)2(H2O)4 M = MnII, FeII both belong to space group P\bar 1, Z = 1, a = 5.194 (3), b = 7.454 (2), c = 8.901 (2) Å, α = 67.07 (2), β = 77.26 (3), γ = 74.46 (4)°, for MnII is shown to have a layer-type structure, where all [HC4O4] units are bonded into infinite chains via symmetric hydrogen bonds, each (HC4O4)2 2− ligand bridging two metal ions (μ-2) in a trans fashion. The structurally most well understood metal squarate M(C4O4)(H2O)4 (M = MnII, FeII, CoII, NiII and ZnII, space group C2/c, Z = 4) is again a polymeric chain with C4O4 2− serving as a bridging ligand between two metal ions (μ-2) in trans positions. A three-dimensional polymeric structure is found to have the formula M(C404)(H2O)2, where C4O4 2− is a bridging ligand between four metal ions (μ-4). Due to the slight difference in packing, there are two structure types in this category: one is in space group R{\bar 3} [M = FeII, a = 11.440 (2), c = 14.504 (3) Å, Z = 9], the other is in Pn{\bar 3}n [M = CoII, a = 16.255 (3) Å, Z = 24]. The structural relationship between all these structures relies heavily on the understanding of intra- and intermolecular hydrogen bonds. The interesting building blocks of each compound will be illustrated. There are tunnels of various sizes in all these structures.


Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 969
Author(s):  
Anurag Kawde ◽  
Mahmoud Sayed ◽  
Qi Shi ◽  
Jens Uhlig ◽  
Tönu Pullerits ◽  
...  

This study demonstrates the use of a photoelectrochemical device comprising earth-abundant hematite photoanode for the oxidation of 5-hydroxymethylfurfural (5-HMF), a versatile bio-based platform chemical, under ambient conditions in the presence of an electron mediator. The results obtained in this study showed that the hematite photoanode, upon doping with fluorine, can oxidize water even at lower pH (4.5 and 9.0). For 5-HMF oxidation, three different pH conditions were investigated, and complete oxidation to 2,5-furandicarboxylic acid (FDCA) via 5-hydroxymethyl-2-furancarboxylic acid (HMFCA) was achieved at pH above 12. At lower pH, the oxidation followed another route via 2,5-diformylfuran (DFF), yielding 5-formyl-2-furancarboxylic acid (FFCA) as the main product. Using the oxidized intermediates as substrates showed DFF to be most efficiently oxidized to FDCA. We also show that, at pH 4.5, the addition of the laccase enzyme promoted the oxidation of 5-HMF to FFCA.


2018 ◽  
Vol 74 (8) ◽  
pp. 1042-1048
Author(s):  
Ouahida Zeghouan ◽  
Mohamed AbdEsselem Dems ◽  
Seifeddine Sellami ◽  
Hocine Merazig ◽  
Jean Claude Daran

The synthesis and characterization of diaquabis[2-(2-hydroxyethyl)pyridine-κ2 N,O)nickel(II) dinitrate, [Ni(C7H9NO)2(H2O)2](NO3)2, under ambient conditions is reported and compared with catena-poly[[bis[2-(2-hydroxyethyl)pyridine-κ2 N,O]copper(II)]-μ-sulfato-κ2 O:O′], [Cu(C7H9NO)2(SO4)] n [Zeghouan et al. (2016). Private communication (refcode 1481676). CCDC, Cambridge, England]. In the two complexes, the 2-(2-hydroxyethyl)pyridine ligands coordinate the metal ions through the N atom of the pyridine ring and the O atom of the hydroxy group, creating a chelate ring. The NiII or CuII ion lies on an inversion centre and exhibits a slightly distorted MO4N2 octahedral coordination geometry, build up by O and N atoms from two 2-(2-hydroxyethyl)pyridine ligands and two water molecules or two O atoms belonging to sulfate anions. The sulfate anion bridges the CuII ions, forming a polymeric chain. The photoluminescence properties of these complexes have been studied on as-synthesized samples and reveal that both compounds display a strong blue-light emission with maxima around 497 nm. From DFT/TDDFT studies, the blue emission appears to be derived from the ligand-to-metal charge-transfer (LMCT) excited state. In addition, the IR spectroscopic properties and thermogravimetric behaviours of both complexes have been investigated.


1997 ◽  
Vol 161 ◽  
pp. 23-47 ◽  
Author(s):  
Louis J. Allamandola ◽  
Max P. Bernstein ◽  
Scott A. Sandford

AbstractInfrared observations, combined with realistic laboratory simulations, have revolutionized our understanding of interstellar ice and dust, the building blocks of comets. Since comets are thought to be a major source of the volatiles on the primative earth, their organic inventory is of central importance to questions concerning the origin of life. Ices in molecular clouds contain the very simple molecules H2O, CH3OH, CO, CO2, CH4, H2, and probably some NH3and H2CO, as well as more complex species including nitriles, ketones, and esters. The evidence for these, as well as carbonrich materials such as polycyclic aromatic hydrocarbons (PAHs), microdiamonds, and amorphous carbon is briefly reviewed. This is followed by a detailed summary of interstellar/precometary ice photochemical evolution based on laboratory studies of realistic polar ice analogs. Ultraviolet photolysis of these ices produces H2, H2CO, CO2, CO, CH4, HCO, and the moderately complex organic molecules: CH3CH2OH (ethanol), HC(= O)NH2(formamide), CH3C(= O)NH2(acetamide), R-CN (nitriles), and hexamethylenetetramine (HMT, C6H12N4), as well as more complex species including polyoxymethylene and related species (POMs), amides, and ketones. The ready formation of these organic species from simple starting mixtures, the ice chemistry that ensues when these ices are mildly warmed, plus the observation that the more complex refractory photoproducts show lipid-like behavior and readily self organize into droplets upon exposure to liquid water suggest that comets may have played an important role in the origin of life.


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