Interhalide ion formation resulting from the freezing of dilute solutions containing components found in natural sea salt are investigated as a potential mechanism for the release of interhalogens to the polar atmosphere. Acidified solutions containing iodide, bromide, and nitrite ions have been frozen and then thawed, with changes in speciation analyzed using UV-visible spectrophotometry. The freezing process is shown to induce the formation of the important interhalide ion, IBr(2)(-). This species has previously been predicted to be a precursor of iodine monobromide, IBr, and represents a potentially important source of halogen atoms in the polar marine boundary layer. The reaction mechanisms that lead to the formation of IBr(2)(-) under freezing conditions are explored using both experimental and computational methodologies. The chemistry involved was subsequently modified in order to mimic naturally occurring conditions more closely and also incorporated the use of hydrogen peroxide as an oxidant. In contrast to previous studies, the freeze-induced production of IBr(2)(-) was thereby observed to occur up to pH <5.1, where the acidity levels are comparable to those found in the polar snowpack.
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http://dx.doi.org/10.1021/jp104910p | DOI Listing |
ACS Appl Mater Interfaces
February 2022
Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, Massachusetts 02139, United States.
Li-O batteries can provide significantly higher gravimetric energy density than Li-ion batteries, but their practical use is limited by a number of fundamental issues associated with oxidizing discharge products such as LiO and LiOH during charging. Soluble inorganic redox mediators (RMs) like LiI and LiBr have been shown to enhance round-trip efficiency where different solvents can greatly shift the redox potential of the RMs, significantly altering the overpotential during charging, as well as their oxidizing power against the discharge product. Unfortunately, other design requirements like (electro)chemical stability with the electrode as well as reactive discharge products greatly constrain the selection of solvent, making it impractical to additionally design the solvent to provide optimal RM performance.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2018
Fachbereich Biologie, Chemie, Pharmazie, Institut für Chemie und Biochemie - Anorganische Chemie, FU Berlin, Fabeckstrasse 34/36, 14195, Berlin, Germany.
Due to a more distinct σ-hole, BrCl is able to form stronger halogen bonds than those in polyhalogen anions based on Cl and Br . This stabilization allows the crystallographic characterization of a variety of new polyinterhalides, in which chloride functions as the central ion as shown by the molecular structures of [AsPh ][Cl(BrCl) ] and [CCl(NMe ) ][Cl(BrCl) ]. Furthermore, the solid-state structure of an octahedrally coordinated nonclassical interhalide is reported for the first time.
View Article and Find Full Text PDFActa Crystallogr C Struct Chem
December 2017
Catalysis Research Center & Department of Chemistry, Technische Universität München, Ernst-Otto-Fischer-Strasse 1, D-85747 Garching b. München, Germany.
A monomeric Pd complex bearing a mixed carbocyclic/N-heterocyclic carbene ligand and two bromides was reacted with an excess of elemental iodine, which resulted in the surprising removal of one bromide ligand and dimerization of the mixed-carbene complex to form di-μ-bromido-bis{[1-(cyclohepta-2,4,6-trien-2-yl-1-ylidene-κC)-3-(2,6-diisopropylphenyl)imidazol-2-ylidene]palladium(II)} bis(pentaiodide) dichloromethane monosolvate, [PdBr(CHN)](I)·CHCl. The dimeric complex features a slightly distorted square-planar core of two Pd centres bridged by two bromide ligands, which lie in the same plane as the seven- and five-membered rings of the bidentate carbene ligand. The counter-ions in the single crystal were found to be pentaiodide monoanions featuring their typical V-shape, whereas for the bulk material, a mixture of Br/I interhalides is proposed.
View Article and Find Full Text PDFAnal Chem
February 2016
School of Chemistry, Monash University, Clayton, VIC 3800, Australia.
The electrochemical behavior of iodine remains a contemporary research interest due to the integral role of the I(-)/I3(-) couple in dye-sensitized solar cell technology. The neutral (I2) and positive (I(+)) oxidation states of iodine are known to be strongly electrophilic, and thus the I(-)/I2/I(+) redox processes are sensitive to the presence of nucleophilic chloride or bromide, which are both commonly present as impurities in nonhaloaluminate room temperature ionic liquids (ILs). In this study, the electrochemistry of I(-), I2, and ICl has been investigated by cyclic voltammetry at a platinum macrodisk electrode in a binary IL mixture composed of 1-butyl-3-methylimidazolium chloride ([C4mim]Cl) and 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C2mim][NTf2]).
View Article and Find Full Text PDFAcc Chem Res
November 2013
Department of Chemistry and Environmental Research Institute, University College Cork, Cork, Ireland.
The knowledge that the freezing process can accelerate certain chemical reactions has been available since the 1960s, particularly in relation to the food industry. However, investigations into such effects on environmentally relevant reactions have only been carried out since the late 1980s. Some 20 years later, the field has matured and scientists have conducted research into various important processes such as the oxidation of nitrite ions to nitrates, sulfites to sulfates, and elemental mercury to inorganic mercury.
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