Fluoride Abstraction Induced by Tris(pentafluoroethyl)difluorophosphorane: A Convenient Way to Synthesize Cationic N-Heterocyclic Carbene- and Cyclic (Alkyl)(amino)carbene-Ligated Copper Alkyne and Arene Complexes.

We herein report the convenient synthesis of different N-heterocyclic carbene (NHC)- and cyclic (alkyl)(amino)carbene (cAAC)-ligated copper cations using the weakly coordinating tris(pentafluoroethyl)trifluorophosphate counterion (FAP anion, [(C2F5)3PF3]-). The reaction of the fluorido complexes [(carbene)CuF] (carbene = NHC, cAACMe) 2a-2f and the tris(pentafluoroethyl)difluorophosphorane (C2F5)3PF2 in the presence of alkynes or arenes led to fluoride transfer from Cu to the phosphorane with formation of the cationic transition metal complexes [(carbene)Cu(L)]+ and the weakly coordinating counteranion [(C2F5)3PF3]- (FAP). Using this method, the complexes [(IDipp)Cu(L)]+FAP- (IDipp = 1,3-bis(2,6-di-iso-propylphenyl)-imidazolin-2-ylidene; L = PhC≡CPh, 4d; PhC≡CMe, 5d), [(cAACMe)Cu(L)]+FAP- (cAACMe = 1-(2,6-di-iso-propylphenyl)-3,3,5,5-tetramethyl-pyrrolidin-2-ylidene; L = PhC≡CPh, 4f; PhC≡CMe, 5f), [(SIDipp)Cu(C6Me6)]+FAP- (6e), (SIDipp = 1,3-bis(2,6-di-iso-propylphenyl)-imidazolidine-2-ylidene), and [(cAACMe)Cu(C6Me6)]+FAP- (6f) have been synthesized and characterized. The complexes [(IDipp)Cu(C6Me6)]+FAP- (6d) and [(cAACMe)Cu(C6Me6)]+FAP- (6f) have been used as catalysts for the copper(I)-catalyzed cycloaddition of benzyl azide to terminal alkynes.

An easy-to-perform evaluation of steric properties of Lewis acids.

Steric and electronic effects play a very important role in chemistry, as these effects influence the shape and reactivity of molecules. Herein, an easy-to-perform approach to assess and quantify steric properties of Lewis acids with differently substituted Lewis acidic centers is reported. This model applies the concept of the percent buried volume (%V Bur) to fluoride adducts of Lewis acids, as many fluoride adducts are crystallographically characterized and are frequently calculated to judge fluoride ion affinities (FIAs). Thus, data such as cartesian coordinates are often easily available. A list of 240 Lewis acids together with topographic steric maps and cartesian coordinates of an oriented molecule suitable for the SambVca 2.1 web application is provided, together with different FIA values taken from the literature. Diagrams of %V Bur as a scale for steric demand vs. FIA as a scale for Lewis acidity provide valuable information about stereo-electronic properties of Lewis acids and an excellent evaluation of steric and electronic features of the Lewis acid under consideration. Furthermore, a novel LAB-Rep model (Lewis acid/base repulsion model) is introduced, which judges steric repulsion in Lewis acid/base pairs and helps to predict if an arbitrary pair of Lewis acid and Lewis base can form an adduct with respect to their steric properties. The reliability of this model was evaluated in four selected case studies, which demonstrate the versatility of this model. For this purpose, a user-friendly Excel spreadsheet was developed and is provided in the ESI, which works with listed buried volumes of Lewis acids %V Bur_LA and of Lewis bases %V Bur_LB, and no results from experimental crystal structures or quantum chemical calculations are necessary to evaluate steric repulsion in these Lewis acid/base pairs.

Tris(pentafluoroethyl)difluorophosphorane: A Versatile Fluoride Acceptor for Transition Metal Chemistry.

Fluoride abstraction from different types of transition metal fluoride complexes [Ln MF] (M=Ti, Ni, Cu) by the Lewis acid tris(pentafluoroethyl)difluorophosphorane (C2 F5 )3 PF2 to yield cationic transition metal complexes with the tris(pentafluoroethyl)trifluorophosphate counterion (FAP anion, [(C2 F5 )3 PF3 ]- ) is reported. (C2 F5 )3 PF2 reacted with trans-[Ni(iPr2 Im)2 (ArF )F] (iPr2 Im=1,3-diisopropylimidazolin-2-ylidene; ArF =C6 F5 , 1 a; 4-CF3 -C6 F4 , 1 b; 4-C6 F5 -C6 F4 , 1 c) through fluoride transfer to form the complex salts trans-[Ni(iPr2 Im)2 (solv)(ArF )]FAP (2 a-c[solv]; solv=Et2 O, CH2 Cl2 , THF) depending on the reaction medium. In the presence of stronger Lewis bases such as carbenes or PPh3 , solvent coordination was suppressed and the complexes trans-[Ni(iPr2 Im)2 (PPh3 )(C6 F5 )]FAP (trans-2 a[PPh3 ]) and cis-[Ni(iPr2 Im)2 (Dipp2 Im)(C6 F5 )]FAP (cis-2 a[Dipp2 Im]) (Dipp2 Im=1,3-bis(2,6-diisopropylphenyl)imidazolin-2-ylidene) were isolated. Fluoride abstraction from [(Dipp2 Im)CuF] (3) in CH2 Cl2 or 1,2-difluorobenzene led to the isolation of [{(Dipp2 Im)Cu}2 ]2+ 2 FAP- (4). Subsequent reaction of 4 with PPh3 and different carbenes resulted in the complexes [(Dipp2 Im)Cu(LB)]FAP (5 a-e, LB=Lewis base). In the presence of C6 Me6 , fluoride transfer afforded [(Dipp2 Im)Cu(C6 Me6 )]FAP (5 f), which serves as a source of [(Dipp2 Im)Cu)]+ . Fluoride abstraction of [Cp2 TiF2 ] (7) resulted in the formation of dinuclear [FCp2 Ti(µ-F)TiCp2 F]FAP (8) (Cp=η5 -C5 H5 ) with one terminal fluoride ligand at each titanium atom and an additional bridging fluoride ligand.

An Investigation of the Symmetric and Asymmetric Cleavage Products in the System Aluminum Trihalide/1-Butylimidazole.

Mixtures of AlX3 (X=Cl, Br) with 1-butylimidazole (BuIm) in various ratios were investigated. The mixtures were characterized by multinuclear (1 H, 27 Al, 13 C, and 15 N) NMR, IR, and Raman spectroscopy and in part by single-crystal X-ray diffraction. Depending on the molar fraction x(AlBr3 ) of the AlBr3 -based mixtures, the cationic aluminum complexes [Al(BuIm)6 ]3+ and [AlBr2 (BuIm)4 ]+ , the neutral adduct [AlBr3 (BuIm)], as well as the anions Br- , [AlBr4 ]- , and [Al2 Br7 ]- could be identified as the products of the symmetric and asymmetric cleavage of dimeric Al2 Br6 . Furthermore, there are hints at the formation of [AlBr2 (BuIm)2 ]+ or related cations. Comparison of the AlBr3 /BuIm system with AlCl3 -based mixtures revealed the influence of the halide: In contrast to AlBr3 , the trication [Al(BuIm)6 ]3+ could not be detected as main product in a 1:6 mixture of AlCl3 and BuIm. Additionally, [AlCl3 (BuIm)] crystallizes from a mixture with x(AlCl3 )=0.60 at room temperature, whereas the corresponding AlBr3 -based mixture remains liquid even at +6 °C. Three AlBr3 -based mixtures are liquid at room temperature, whereas all other mixtures are solids with melting points between 46 and 184 °C. The three liquid mixtures exhibit medium to high viscosities (117 to >1440 mPa s), low conductivities (0.03-0.20 mS cm-1 ), but high densities (1.80-2.21 g cm-3 ). Aluminum could be successfully deposited from one of the neat Lewis acidic mixtures of the AlBr3 -based system.