scholarly journals Water cluster in hydrophobic crystalline porous covalent organic frameworks

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ke Tian Tan ◽  
Shanshan Tao ◽  
Ning Huang ◽  
Donglin Jiang
Keyword(s):  
Water Cluster ◽  
Water Exchange ◽  
Capillary Condensation ◽  
Water Molecules ◽  
Covalent Organic Frameworks ◽  
High Uptake ◽  
One Dimensional ◽  
The Past ◽  
Low Pressures ◽  
Small Hydrophobic

AbstractProgress over the past decades in water confinement has generated a variety of polymers and porous materials. However, most studies are based on a preconception that small hydrophobic pores eventually repulse water molecules, which precludes the exploration of hydrophobic microporous materials for water confinement. Here, we demonstrate water confinement across hydrophobic microporous channels in crystalline covalent organic frameworks. The frameworks are designed to constitute dense, aligned and one-dimensional polygonal channels that are open and accessible to water molecules. The hydrophobic microporous frameworks achieve full occupation of pores by water via synergistic nucleation and capillary condensation and deliver quick water exchange at low pressures. Water confinement experiments with large-pore frameworks pinpoint thresholds of pore size where confinement becomes dominated by high uptake pressure and large exchange hysteresis. Our results reveal a platform based on microporous hydrophobic covalent organic frameworks for water confinement.

scholarly journals Evaluating the performance of multivariate indicators of resilience loss

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Els Weinans ◽  
Rick Quax ◽  
Egbert H. van Nes ◽  
Ingrid A. van de Leemput
Keyword(s):  
Time Series ◽  
Complex Systems ◽  
Multivariate Time Series ◽  
Tipping Points ◽  
Physical And Mental Health ◽  
One Dimensional ◽  
Slowing Down ◽  
The Past ◽  
Technological Developments ◽  
Resilience Indicators

AbstractVarious complex systems, such as the climate, ecosystems, and physical and mental health can show large shifts in response to small changes in their environment. These ‘tipping points’ are notoriously hard to predict based on trends. However, in the past 20 years several indicators pointing to a loss of resilience have been developed. These indicators use fluctuations in time series to detect critical slowing down preceding a tipping point. Most of the existing indicators are based on models of one-dimensional systems. However, complex systems generally consist of multiple interacting entities. Moreover, because of technological developments and wearables, multivariate time series are becoming increasingly available in different fields of science. In order to apply the framework of resilience indicators to multivariate time series, various extensions have been proposed. Not all multivariate indicators have been tested for the same types of systems and therefore a systematic comparison between the methods is lacking. Here, we evaluate the performance of the different multivariate indicators of resilience loss in different scenarios. We show that there is not one method outperforming the others. Instead, which method is best to use depends on the type of scenario the system is subject to. We propose a set of guidelines to help future users choose which multivariate indicator of resilience is best to use for their particular system.

2D Self-assembly and Electronic Characterization of Oxygen-Boron-Oxygen-Doped Chiral Graphene Nanoribbons

2021 ◽  
Author(s):  
Lei Jin ◽  
Nerea Bilbao ◽  
Yang Lv ◽  
Xiao-Ye Wang ◽  
Soltani Paniz ◽  
...  
Keyword(s):  
Edge Effects ◽  
Self Assembly ◽  
Quantum Confinement ◽  
Graphene Nanoribbons ◽  
One Dimensional ◽  
The Past ◽  
Different Types

Graphene nanoribbons (GNRs), quasi-one-dimensional strips of graphene, exhibit a nonzero bandgap due to quantum confinement and edge effects. In the past decade, different types of GNRs with atomically precise structures...

The Structure of Emotional Response: 1984 Presidential Candidates

1988 ◽  
Vol 82 (3) ◽  
pp. 737-761 ◽  
Author(s):  
George E. Marcus
Keyword(s):  
Emotional Response ◽  
Two Dimensions ◽  
Negative Emotionality ◽  
One Dimensional ◽  
Presidential Candidates ◽  
The Past ◽  
Emotional Appraisal ◽  
Psychological Models ◽  
Dimensional Models ◽  
Feeling Thermometer

Over the past two decades psychological models of affect have changed from valence (one-dimensional) models to multiple-dimensional models. The most recent models, circumplex models, are two-dimensional. Feeling thermometer measures, which derive their theoretical logic from earlier (valence) models of emotional appraisal, are shown to be confounded. Underlying the variation obtained using feeling thermometer measures are two dimensions of emotional response, mastery (positive emotionality) and threat (negative emotionality). Analysis of the 1984 NES survey suggests that positive emotional response is twice as influential as negative emotional response in predicting presidential candidate vote disposition to the presidential candidates. Reliance on emotional response is shown to be uniformly influential across various strata of the electorate.Policy considerations have little direct influence on vote disposition, though policy considerations are indirectly related to vote disposition through the influence of issues on the degree of feelings of threat evoked by the candidates.

scholarly journals Two New Polyiodides in the 4,4´-Bipyridinium Diiodide/Iodine System

2012 ◽  
Vol 67 (1) ◽  
pp. 5-10
Author(s):  
Guido J. Reiss ◽  
Martin van Megen
Keyword(s):  
Hydrogen Bonding ◽  
Hydrogen Bonds ◽  
Complex I ◽  
The Other ◽  
Cyclic Dimer ◽  
Water Molecules ◽  
Spectroscopic Methods ◽  
Halogen Bonds ◽  
One Dimensional ◽  
Hydroiodic Acid

The reaction of bipyridine with hydroiodic acid in the presence of iodine gave two new polyiodide-containing salts best described as 4,4´-bipyridinium bis(triiodide), C10H10N2[I3]2, 1, and bis(4,4´-bipyridinium) diiodide bis(triiodide) tris(diiodine) solvate dihydrate, (C10H10N2)2I2[I3]2 · 3 I2 ·2H2O, 2. Both compounds have been structurally characterized by crystallographic and spectroscopic methods (Raman and IR). Compound 1 is composed of I3 − anions forming one-dimensional polymers connected by interionic halogen bonds. These chains run along [101] with one crystallographically independent triiodide anion aligned and the other triiodide anion perpendicular to the chain direction. There are no classical hydrogen bonds present in 1. The structure of 2 consists of a complex I144− anion, 4,4´-bipyridinium dications and hydrogen-bonded water molecules in the ratio of 1 : 2 : 2. The I144− polyiodide anion is best described as an adduct of two iodide and two triiodide anions and three diiodine molecules. Two 4,4´-bipyridinium cations and two water molecules form a cyclic dimer through N-H· · ·O hydrogen bonds. Only weak hydrogen bonding is found between these cyclic dimers and the polyiodide anions.

The hidden layers of microbial community structure: extracting the concealed diversity dimensions from our sequencing data

2020 ◽  
Vol 367 (11) ◽  
Author(s):  
Andrea Fasolo ◽  
Laura Treu ◽  
Piergiorgio Stevanato ◽  
Giuseppe Concheri ◽  
Stefano Campanaro ◽  
...  
Keyword(s):  
Sequencing Data ◽  
16S Sequencing ◽  
Evolutionary Aspect ◽  
One Dimensional ◽  
Sequence Identity ◽  
The Past ◽  
Environmental Processes ◽  
Final Layer ◽  
Evolutionary Success ◽  
Microbial Groups

ABSTRACT Microbial metabarcoding is the standard approach to assess communities’ diversity. However reports are often limited to simple OTU abundances for each phylum, giving rather one-dimensional views of microbial assemblages, overlooking other accessible aspects. The first is masked by databases incompleteness; OTU picking involves clustering at 97% (near-species) sequence identity, but different OTUs regularly end up under a same taxon name. When expressing diversity as number of obtained taxonomical names, a large portion of the real diversity lying within the data remains underestimated. Using the 16S sequencing results of an environmental transect across a gradient of 17 coastal habitats we first extracted the number of OTUs hidden under the same name. Further, we observed which was the deepest rank yielded by annotation, revealing for which microbial groups are we missing most knowledge. Data were then used to infer an evolutionary aspect: what is, in each phylum the success of the present time individuals (abundances for each OTU) in relation to their prior evolutionary success in differentiation (number of OTUs). This information reveals whether the past speciation/diversification force is matched by the present competitiveness in reproduction/persistence. The final layer explored is functional diversity, i.e. abundances of groups involved in specific environmental processes.

Size and shape-controlled synthesis of Ru nanocrystals

2018 ◽  
Vol 3 (12) ◽  
Author(s):  
Linlin Xu ◽  
Jun Yang
Keyword(s):  
Noble Metal ◽  
Chemical Properties ◽  
Controlled Synthesis ◽  
One Dimensional ◽  
Size And Shape ◽  
The Past ◽  
Metal Nanomaterials ◽  
Shape Controlled ◽  
Synthetic Approaches ◽  
Coherent Picture

Abstract Mastery over the size/shape of nanocrystals (NCs) enables control of their properties and enhancement of their usefulness for a given application. Within the past decades, the development of wet-chemistry methods leads to the blossom of research in noble metal nanomaterials with tunable sizes and shapes. We herein would prefer to devote this chapter to introduce the solution-based methods for size and shape-controlled synthesis of ruthenium (Ru) NCs, which can be summarized into five categories: (i) Synthesis of spherical Ru NCs; (ii) synthesis of one-dimensional (1D) Ru NCs, e.g. wires and rods; (iii) synthesis of two-dimensional (2D) Ru NCs, e.g. nanoplates; (iv) synthesis of Ru NCs with hollow interiors and (v) synthesis of Ru NCs with other morphologies, e.g. chains, dendrites and branches. We aim at highlighting the synthetic approaches and growth mechanisms of these types of Ru NCs. We also introduce the detailed characterization tools for analysis of Ru NCs with different sizes/shapes. With respect to the creation of great opportunities and tremendous challenges due to the accumulation in noble metal nanomaterials, we briefly make some perspectives for the future development of Ru NCs so as to provide the readers a systematic and coherent picture of this promising field. We hope this reviewing effort can provide for technical bases for effectively designing and producing Ru NCs with enhanced physical/chemical properties. Graphical Abstract: The solution-based methods for size and shape-controlled synthesis of ruthenium nanocrystals as well as the mechanisms behind them are extensively reviewed.

Syntheses and crystal structures of two magnesium–tetrazole compounds in salt and polymeric forms

2015 ◽  
Vol 71 (3) ◽  
pp. 222-228 ◽  
Author(s):  
Mohamed Abdellatif Bensegueni ◽  
Aouatef Cherouana ◽  
Slimane Dahaoui
Keyword(s):  
Alkaline Earth ◽  
Three Dimensional ◽  
Polymer Chains ◽  
Magnesium Ion ◽  
Water Molecules ◽  
Compound I ◽  
Hydrothermal Conditions ◽  
One Dimensional ◽  
Polymeric Chains ◽  
Hydrogen Bonded

Two alkaline earth–tetrazole compounds, namelycatena-poly[[[triaquamagnesium(II)]-μ-5,5′-(azanediyl)ditetrazolato-κ3N1,N1′:N5] hemi{bis[μ-5,5′-(azanediyl)ditetrazolato-κ3N1,N1′:N2]bis[triaquamagnesium(II)]} monohydrate], {[Mg(C2HN9)(H2O)3][Mg2(C2HN9)2(H2O)6]0.5·H2O}n, (I), and bis[5-(pyrazin-2-yl)tetrazolate] hexaaquamagnesium(II), (C5H3N6)[Mg(H2O)6], (II), have been prepared under hydrothermal conditions. Compound (I) is a mixed dimer–polymer based on magnesium ion centres and can be regarded as the first example of a magnesium–tetrazolate polymer in the crystalline form. The structure shows a complex three-dimensional hydrogen-bonded network that involves magnesium–tetrazolate dimers, solvent water molecules and one-dimensional magnesium–tetrazolate polymeric chains. The intrinsic cohesion in the polymer chains is ensured by N—H...N hydrogen bonds, which formR22(7) rings, thus reinforcing the propagation of the polymer chain along theaaxis. The crystal structure of magnesium tetrazole salt (II) reveals a mixed ribbon of hydrogen-bonded rings, of typesR22(7),R22(9) andR24(10), running along thecaxis, which are linked byR24(16) rings, generating a 4,8-cflunet.

scholarly journals Synthesis and crystal structure of a 6-chloronicotinate salt of a one-dimensional cationic nickel(II) coordination polymer with 4,4′-bipyridine

2020 ◽  
Vol 76 (5) ◽  
pp. 599-604
Author(s):  
Nives Politeo ◽  
Mateja Pisačić ◽  
Marijana Đaković ◽  
Vesna Sokol ◽  
Boris-Marko Kukovec
Keyword(s):  
Molecular Structure ◽  
Coordination Polymer ◽  
Three Dimensional ◽  
Polymeric Chain ◽  
Water Molecules ◽  
Sulfate Heptahydrate ◽  
Synthesis And Crystal Structure ◽  
One Dimensional ◽  
Polymeric Chains ◽  
Hydrogen Bonded

A 6-chloronicotinate (6-Clnic) salt of a one-dimensional cationic nickel(II) coordination polymer with 4,4′-bipyridine (4,4′-bpy), namely, catena-poly[[[tetraaquanickel(II)]-μ-4,4′-bipyridine-κ2 N:N′] bis(6-chloronicotinate) tetrahydrate], {[Ni(C10H8N2)(H2O)4](C6H3ClNO2)2·4H2O} n or {[Ni(4,4′-bpy)(H2O)4](6-Clnic)2·4H2O} n , (1), was prepared by the reaction of nickel(II) sulfate heptahydrate, 6-chloronicotinic acid and 4,4′-bipyridine in a mixture of water and ethanol. The molecular structure of 1 comprises a one-dimensional polymeric {[Ni(4,4′-bpy)(H2O)4]2+} n cation, two 6-chloronicotinate anions and four water molecules of crystallization per repeating polymeric unit. The nickel(II) ion in the polymeric cation is octahedrally coordinated by four water molecule O atoms and by two 4,4′-bipyridine N atoms in the trans position. The 4,4′-bipyridine ligands act as bridges and, thus, connect the symmetry-related nickel(II) ions into an infinite one-dimensional polymeric chain extending along the b-axis direction. In the extended structure of 1, the polymeric chains of {[Ni(4,4′-bpy)(H2O)4]2+} n , the 6-chloronicotinate anions and the water molecules of crystallization are assembled into an infinite three-dimensional hydrogen-bonded network via strong O—H...O and O—H...N hydrogen bonds, leading to the formation of the representative hydrogen-bonded ring motifs: tetrameric R 2 4(8) and R 4 4(10) loops, a dimeric R 2 2(8) loop and a pentameric R 4 5(16) loop.

scholarly journals The trend of the oxidants in boreal forest over 2007–2018: comprehensive modelling study with long-term measurements at SMEAR II, Finland

2020 ◽  
Author(s):  
Dean Chen ◽  
Putian Zhou ◽  
Tuomo Nieminen ◽  
Pontus Roldin ◽  
Ximeng Qi ◽  
...  
Keyword(s):  
Air Pollutants ◽  
Size Range ◽  
Chemical Components ◽  
Detailed Model ◽  
One Dimensional ◽  
The Past ◽  
Main Driver ◽  
The One ◽  
Long Term Trend

Abstract. Major atmospheric oxidants (OH, O3 and NO3) dominate the atmospheric oxidation capacity, while H2SO4 is considered as a main driver for new particle formation events. Although numerous studies have investigated the long-term trend of ozone in Europe, the trend of OH, NO3 and H2SO4 at specific sites are to a large extent unknown. In this study, we investigated how the trends in major atmospheric oxidants (OH, O3 and NO3) and H2SO4 changed in southern Finland during the past 12 years and discuss how these trends relate to decreasing emissions of regulated air pollutants in Europe. The one-dimensional model SOSAA has been applied in several studies at the SMEAR II station, and has been validated by measurements in several projects. Here, we ran the SOSAA model for the years 2007–2018 to simulate the atmospheric chemical components, especially the atmospheric oxidants and H2SO4 at SMEAR II. The simulations were evaluated with observations at SMEAR II for several shorter and longer campaigns. Our results show that OH increased by +1.56 (−0.8; +3.17) % yr−1 during daytime and NO3 decreased by −3.92 (−6.49; −1.79) % yr−1 during nighttime, indicating different trends of the oxidants during day and night. Sulphuric acid decreased during daytime by −5.12 (−11.39; −0.52) % yr−1, which correlated with the observed decreasing concentration of newly formed particles in the size range 3–25 nm by 1.4 % yr−1 at SMEAR II during the years 1997–2012 (Nieminen et al., 2014). Additionally we compared our simulated OH, NO3 and H2SO4 concentrations with proxies, which are commonly applied in case limited amount of parameters are measured and no detailed model simulations are available.

(NH4)[B3PO6(OH)3]·0.5H2O

2007 ◽  
Vol 63 (11) ◽  
pp. i185-i185 ◽  
Author(s):  
Wei Liu ◽  
Jingtai Zhao
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bond ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
Water Molecules ◽  
Hydrogen Bond Network ◽  
Ammonium Ions ◽  
One Dimensional ◽  
Bond Network ◽  
Solvothermal Conditions

The title compound, ammonium catena-[monoboro-monodihydrogendiborate-monohydrogenphosphate] hemihydrate, was obtained under solvothermal conditions using glycol as the solvent. The crystal structure is constructed of one-dimensional infinite borophosphate chains, which are interconnected by ammonium ions and water molecules via a complex hydrogen-bond network to form a three-dimensional structure. The water molecules of crystallization are disordered over inversion centres, and their H atoms were not located.

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