Silver(i) Perfluoroalcoholates: Synthesis, Structure, and their Use as Transfer Reagents.

Herein we report a general access to silver(i) perfluoroalcoholates, their structure in the solid state and in solution, and their use as transfer reagents. The silver(i) perfluoroalcoholates are prepared by the reaction of AgF with the corresponding perfluorinated carbonyl compounds in acetonitrile and are stable for a prolonged time at -18 °C. X-ray analysis of single crystals of perfluoroalcoholate species showed that two Ag(i) centers are bridged by the alcoholate ligands. In acetonitrile solution, Ag[OCF3] forms different structures as indicated by IR spectroscopy. Furthermore, the silver(i) perfluoroalcoholates can be used as easy-to-handle transfer reagents for the synthesis of Cu[OCF3], Cu[OC2F5], [PPh4][Au(CF3)3(OCF3)], and fluorinated alkyl ethers.

Catalyst-Free Trifluoromethoxylation of Silyl Enol Ethers and Allyl Silanes with Bis(trifluoromethyl)peroxide.

Radical trifluoromethoxylation is an attractive approach to prepare compounds featuring the important OCF3 group, however most existing methods have focused on aromatic substrates. Here, we report novel methodologies with alkenyl substrates employing bis(trifluoromethyl)peroxide (BTMP) as a practical and comparatively atom economical trifluoromethoxylating reagent. With silyl enol ether substrates, switching reaction solvent allows for the synthesis of either α-(trifluoromethoxy)ketone products or unprecedented alkenyl-OCF3 species. Furthermore, allyl silanes have been employed as substrates for the first time, affording allyl(trifluoromethyl)ether products in good yields. In each case, the methods operate at room temperature without large excesses of the alkene substrate while, in contrast to previous radical trifluoromethoxylation reactions, no catalyst, light or other activators are required.

Gold Teflates Revisited: From the Lewis Superacid [Au(OTeF5 )3 ] to the Anion [Au(OTeF5 )4 ].

A new synthetic access to the Lewis acid [Au(OTeF5 )3 ] and the preparation of the related, unprecedented anion [Au(OTeF5 )4 ]- with inorganic or organic cations starting from commercially available and easy-to-handle gold chlorides are presented. In this first extensive study of the Lewis acidity of a transition-metal teflate complex by using different experimental and quantum chemical methods, [Au(OTeF5 )3 ] was classified as a Lewis superacid. The solid-state structure of the triphenylphosphine oxide adduct [Au(OPPh3 )(OTeF5 )3 ] was determined, representing the first structural characterization of an adduct of this highly reactive [Au(OTeF5 )3 ]. Therein, the coordination environment around the gold center slightly deviates from the typical square planar geometry. The [Au(OTeF5 )4 ]- anion shows a similar coordination motif.

Reactivity of [AuF3 (SIMes)]: Pathway to Unprecedented Structural Motifs.

We report on a comprehensive reactivity study starting from [AuF3 (SIMes)] to synthesize different motifs of monomeric gold(III) fluorides. A plethora of different ligands has been introduced in a mono-substitution yielding trans-[AuF2 X(SIMes)] including alkynido, cyanido, azido, and a set of perfluoroalkoxido complexes. The latter were better accomplished via use of perfluorinated carbonyl-bearing molecules, which is unprecedented in gold chemistry. In case of the cyanide and azide, triple substitution gave rise to the corresponding [AuX3 (SIMes)] complexes. Comparison of the chemical shift of the carbene carbon atom in the 13 C{1 H} NMR spectrum, the calculated SIMes affinity and the Au-C bond length in the solid state with related literature-known complexes yields a classification of trans-influences for a variety of ligands attached to the gold center. Therein, the mixed fluorido perfluoroalkoxido complexes have a similar SIMes affinity to AuF3 with a very low Gibbs energy of formation when using the perfluoro carbonyl route.

The Rise of Trichlorides Enabling an Improved Chlorine Technology.

Chlorine plays a central role for the industrial production of numerous materials with global relevance. More recently, polychlorides have been evolved from an area of academic interest to a research topic with enormous industrial potential. In this minireview, the value of trichlorides for chlorine storage and chlorination reactions are outlined. Particularly, the inexpensive ionic liquid [NEt3 Me][Cl3 ] shows a similar and sometimes even advantageous reactivity compared to chlorine gas, while offering a superior safety profile. Used as a chlorine storage, [NEt3 Me][Cl3 ] could help to overcome the current limitations of storing and transporting chlorine in larger quantities. Thus, trichlorides could become a key technique for the flexibilization of the chlorine production enabling an exploitation of renewable, yet fluctuating, electrical energy. As the loaded storage, [NEt3 Me][Cl3 ], is a proven chlorination reagent, it could directly be employed for downstream processes, paving the path to a more practical and safer chlorine industry.

(Noble Gas)n -NC+ Molecular Ions in Noble Gas Matrices: Matrix Infrared Spectra and Electronic Structure Calculations.

An investigation of pulsed-laser-ablated Zn, Cd and Hg metal atom reactions with HCN under excess argon during co-deposition with laser-ablated Hg atoms from a dental amalgam target also provided Hg emissions capable of photoionization of the CN photo-dissociation product. A new band at 1933.4 cm-1 in the region of the CN and CN+ gas-phase fundamental absorptions that appeared upon annealing the matrix to 20 K after sample deposition, and disappeared upon UV photolysis is assigned to (Ar)n CN+ , our key finding. It is not possible to determine the n coefficient exactly, but structure calculations suggest that one, two, three or four argon atoms can solvate the CN+ cation in an argon matrix with C-N absorptions calculated (B3LYP) to be between 2317.2 and 2319.8 cm-1 . Similar bands were observed in solid krypton at 1920.5, in solid xenon at 1935.4 and in solid neon at 1947.8 cm-1 . H13 CN reagent gave an 1892.3 absorption with shift instead, and a 12/13 isotopic frequency ratio-nearly the same as found for 13 CN+ itself in the gas phase and in the argon matrix. The CN+ molecular ion serves as a useful infrared probe to examine Ng clusters. The following ion reactions are believed to occur here: the first step upon sample deposition is assisted by a focused pulsed YAG laser, and the second step occurs on sample annealing: (Ar)2 + +CN→Ar+CN+ →(Ar)n CN+ .

Synthesis of a Hexachloro Sulfate(IV) Dianion Enabled by Polychloride Chemistry.

The preparation and structural characterization of [NEt3 Me]2 [SCl6 ] is described, which is the first example of a [SCl6 ]2- dianion and of a halosulfate anion of the type [Sx Xy ]z- in general. This dianion belongs to the group of 14-valence electron AB6 E systems and forms an octahedral structure in the solid-state. Interestingly, co-crystallization with CH2 Cl2 affords [NEt3 Me]2 [SCl6 ]⋅4 CH2 Cl2 containing [SCl6 ]2- dianions with C4v symmetry. As suggested by quantum-chemical calculations, the distortion of the structure is not caused by a stereochemically active lone pair but by enhanced hydrogen bonding interactions with CH2 Cl2 . At elevated temperatures, [NEt3 Me]2 [SCl6 ] decomposes to various sulfur chlorine compounds as shown by Raman spectroscopy. Cooling back to room temperature results in the selective formation of [NEt3 Me]2 [SCl6 ] which is comparable to the well-studied SCl4 .

Investigation of Bis(Perfluoro-tert-Butoxy) Halogenates(I/III).

A systematic study of halogenate(I/III) anions with polyatomic ligands is presented. The bis(perfluoro-tert-butoxy) halogenates(I) [X(OC4 F9 )2 ]- , X=Cl, Br, I, of chlorine, bromine, and iodine are prepared as their tetraethylammonium salts and characterized with IR, Raman, and NMR spectroscopic methods, as well as single-crystal X-ray diffraction analyses. Spectroscopical data are supported by quantum-chemical calculations. Additionally, the bonding situation of the species in question are analyzed and discussed. Furthermore, the oxidation to the corresponding halogenate(III) derivatives was studied. For [Br(OC4 F9 )2 ]- , oxidation with elemental fluorine gave [BrF2 (OC4 F9 )2 ]- . Iodide was directly oxidized by ClOC4 F9 to the IIII species [I(OC4 F9 )4 ]- , which is a surprisingly inert anion that might be used as a weakly coordinating anion (WCA) in the future. For [Cl(OC4 F9 )2 ]- , the decomposition products of the synthetic approaches towards a chlorine(III) system were analyzed.

Synthesis and Characterization of Poly(hydrogen halide) Halogenates (-I).

Herein, we report the synthesis and characterization of a variety of novel poly(hydrogen halide) halogenates (-I). The bifluoride ion, which is known to have the highest hydrogen bond energy of ≈160 kJ mol-1 , is the most famous among many examples of [X(HX)n ]- anions (X=F, Cl) known in the literature. In contrast, little is known about poly(hydrogen halide) halogenates containing two different halogens, ([X(HY)n ]- ). In this work we present the synthesis of anions of the type [X(HY)n ]- (X=Br, I, ClO4 ; Y=Cl, Br, CN) stabilized by the [PPh4 ]+ and [PPN]+ cation. The obtained compounds have been characterized by single-crystal X-ray diffraction, Raman spectroscopy and quantum-chemical calculations. In addition, the behavior of halide ions in hydrogen fluoride was investigated by using experimental and quantum-chemical methods in order to gain knowledge on the acidity of hydrogen halides in HF.

Friedel-Crafts Type Methylation with Dimethylhalonium Salts.

The dimethylchloronium salt [Me2 Cl][Al(OTeF5 )4 ] is used to methylate electron-deficient aromatic systems in Friedel-Crafts type reactions as shown by the synthesis of N-methylated cations, such as [MeNC5 F5 ]+ , [MeNC5 F4 I]+ , and [MeN3 C3 F3 ]+ . To gain a better understanding of such fundamental Friedel-Crafts reactions, the role of the dimethylchloronium cation has been evaluated by quantum-chemical calculations.

In Situ Synthesis and Applications for Polyinterhalides Based on BrCl.

The use of neat BrCl in organic and inorganic chemistry is limited due to its gaseous aggregate state and especially its decomposition into Cl2 and Br2 . The stabilization of BrCl in form of reactive ionic liquids via a novel in situ synthesis route shifts this equilibrium drastically to the BrCl side, which leads to safer and easier-to-handle interhalogenation reagents. Furthermore, the crystalline derivatives of the hitherto unknown [Cl(BrCl)2 ]- and [Cl(BrCl)4 ]- anions were synthesized and characterized by single-crystal X-ray diffraction (XRD), Raman and IR spectroscopy, as well as quantum chemical calculations.

[NMe4 ][I4 Br5 ]: A new Iodobromide from an Ionic Liquid with Halogen-Halogen Interactions.

Tetramethylammonium tetraiodopentabromide [NMe4 ][I4 Br5 ] was the first iodobromide to be synthesized and crystallized in an ionic liquid as well as in dichloromethane. The new iodobromides show different structure motives yet are unknown from other nonahalides and can be better described as [(I2 Br3 )- ⋅2 IBr]. The additional IBr units are connected by halogen-halogen interactions on the central V-shaped [I2 Br3 ]- . The characterization was performed by Raman spectroscopy and single crystal X-ray structure determination. Conductivity measurements, thermogravimetric analysis and quantum-chemical calculations completed the structural discussion.

Bichloride-based ionic liquids for the merged storage, processing, and electrolysis of hydrogen chloride.

Hydrogen chloride is produced as a by-product in industrial processes on a million-ton scale. Since HCl is inherently dangerous, its storage and transport are avoided by, e.g., on-site electrolysis providing H2 and Cl2 which usually requires complex cell designs and PFAS-based membranes. Here we report a complementary approach to safely store 0.61 kilogram HCl per kilogram storage material [NEt3Me]Cl forming the bichloride [NEt3Me][Cl(HCl)n]. Although HCl release is possible from this ionic liquid by heat or vacuum, the bichloride can be used directly to produce base chemicals like vinyl chloride. Alternatively, [NEt3Me][Cl(HCl)n] is electrolyzed under anhydrous conditions using a membrane-free cell to generate H2 and the corresponding chlorination agent [NEt3Me][Cl(Cl2)n], enabling the combination of these ionic liquids for the production of base chemicals.

Synthesis of 3-epi-Hypatulin B Featuring a Late-Stage Photo-Oxidation in Flow.

A synthesis of 3-epi-hypatulin B, a highly oxygenated and densely functionalized bicyclic scaffold, is reported. The carbon skeleton was prepared by functionalization of a cyclopentanone and an intramolecular Mukaiyama aldol reaction. Highlights include a late-stage photo-oxidation of a methoxyallene to provide an ester group. The problems encountered in the batch process were solved by translation into a flow protocol. Our synthesis highlights the value of flow chemistry to enable challenging late-stage transformations in natural product synthesis.

Synthesis of Plakortolides E and I Enabled by Base Metal Catalysis.

A protecting-group-free synthesis of two endoperoxide natural products, plakortolide E and plakortolide I, is reported. Key steps are a vanadium-mediated epoxidation, an iron-catalyzed allylic substitution, and a cobalt-induced endoperoxide formation. Our approach combines chemoselective bond-forming reactions and one-pot operations to forge an overall efficient synthesis.

Conductivity and Redox Potentials of Ionic Liquid Trihalogen Monoanions [X3 ]- , [XY2 ]- , and [BrF4 ]- (X=Cl, Br, I and Y=Cl, Br).

The ionic liquid (IL) trihalogen monoanions [N2221 ][X3 ]- and [N2221 ][XY2 ]- ([N2221 ]+ =triethylmethylammonium, X=Cl, Br, I, Y=Cl, Br) were investigated electrochemically via temperature dependent conductance and cyclic voltammetry (CV) measurements. The polyhalogen monoanions were measured both as neat salts and as double salts in 1-butyl-1-methyl-pyrrolidinium trifluoromethane-sulfonate ([BMP][OTf], [X3 ]- /[XY2 ]- 0.5 M). Lighter IL trihalogen monoanions displayed higher conductivities than their heavier homologues, with [Cl3 ]- being 1.1 and 3.7 times greater than [Br3 ]- and [I3 ]- , respectively. The addition of [BMP][OTf] reduced the conductivity significantly. Within the group of polyhalogen monoanions, the oxidation potential develops in the series [Cl3 ]- >[BrCl2 ]- >[Br3 ]- >[IBr2 ]- >[ICl2 ]- >[I3 ]- . The redox potential of the interhalogen monoanions was found to be primarily determined by the central halogen, I in [ICl2 ]- and [IBr2 ]- , and Br in [BrCl2 ]- . Additionally, tetrafluorobromate(III) ([N2221 ]+ [BrF4 ]- ) was analyzed via CV in MeCN at 0 °C, yielding a single reversible redox process ([BrF2 ]- /[BrF4 ]- ).

Novel synthetic pathway for the production of phosgene.

Chloride ions are efficient catalysts for the synthesis of phosgene from carbon monoxide and elemental chlorine at room temperature and atmospheric pressure. Control experiments rule out a radical mechanism and highlight the role of triethylmethylammonium trichloride, [NEt3Me][Cl3], as active species. In the catalytic reaction, commercially available [NEt3Me]Cl reacts with Cl2 to form [NEt3Me][Cl3], enabling the insertion of CO into an activated Cl─Cl bond with a calculated energy barrier of 56.9 to 77.6 kJ mol−1. As [NEt3Me]Cl is also a useful chlorine storage medium, it could serve as a catalyst for phosgene production and as chlorine storage in a combined industrial process.