Metal complexes as potential ligands : the deprotonation of aminephenolate metal complexes

The cationic nickel, copper and zinc complexes of tris-(2-hydroxybenzyl)-aminoethylamine (H6TrenSal) have been deprotonated using potassium hydroxide. The nickel complex can be sequentially deprotonated to form a series of compounds namely, [(H6TrenSal)Ni]+, [(H6TrenSal)Ni] and "[(H6TrenSal)Ni]K". The latter is isolated as a mixture of species namely [{(H6TrenSal)Ni}K(EtOH)]2, [{(H6TrenSal)Ni}K(EtOH)2-μ-OH2]2 and [{(H6TrenSal)Ni}K(EtOH)2-μ-EtOH]2, which co-crystallise in a roughly 50:27.5:22.5 ratio. In contrast the deprotonation of [(H6TrenSal)M]+ (M = Cu, Zn) results in the formation of tetrameric complexes [({(H6TrenSal)Ni}K(OH2)2)4(μ4-OH2)]

Methyl 2-amino-5-iso­propyl-1,3-thia­zole-4-carboxyl­ate

The title compound, C8H12N2O2S, forms a supramolecular network based on N-HN hydrogen-bonded centrosymmetric dimers that are linked in turn by N-HO contacts

Diisopropylamide and TMP turbo-grignard reagents : a structural rationale for their contrasting reactivities

A neutral dimeric molecule in crystal form, the diisopropylamido turbo-Grignard reagent "(iPr2N)MgCl⋅LiCl" (see structure; blue N, red O, green Mg, yellow Cl, black C) separates into several charged ate species in dynamic exchange with each other in THF solution as determined by a combination of EXSY and DOSY NMR studies

N-heterocyclic germylenes: structural characterisation of some heavy analogues of the ubiquitous N-heterocyclic carbenes

The X-ray crystal structures of three N-heterocyclic germylenes (NHGes) have been elucidated including the previously unknown 1,3-bis(2,6-dimethylphenyl)diazagermol-2-ylidene (1). In addition, the X-ray crystal structures of the previously synthesised 1,3-bis(2,4,6-trimethylphenyl)diazagermol-2-ylidene (2) and 1,3-bis(2,6-diisopropylphenyl)diazagermol-2-ylidene (3) are also reported. The discrete molecular structures of compounds 1 to 3 are comparable, with Ge-N bond lengths in the range 1.835-1.875 Å, while the N-Ge-N bond angles range between 83.6 and 85.2°. Compound 2 was compared to the analogous N-heterocyclic carbene species, 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene (IMes). The major geometrical difference observed, as expected, was the bond angle around the divalent group 14 atom. The N-Ge-N bond angle was 83.6° for compound 2 versus the N-C-N bond angle of 101.4° for IMes. The Sn equivalent of (1), 1,3-bis(2,6-dimethylphenyl)diazastannol-2-ylidene (4), has also been synthesised and its crystal structure is reported here. In order to test their suitability as ligands, compounds 1 to 3 were reacted with a wide range of transition metal complexes. No NHGes containing metal complexes were observed. In all cases the NHGe either degraded or gave no reaction

Trans-metal-trapping meets FLP chemistry : Ga(CH2SiMe3)3 induced C-H functionalizations

Merging two topical themes in Main Group chemistry, namely cooperative bimetallics and FLP activity, this Forum Article focuses on the cooperativity-induced outcomes observed when the tris(alkyl)gallium compound GaR3 (R= CH2SiMe3) is paired with lithium amide LiTMP (TMP=2,2,6,6-tetramethylpiperidide) or the sterically hindered NHC ItBu (ItBu = 1,3-bis(tert-butyl)imidazol-2-ylidene). Drawing together some previously published work with new results, unique tandem reactivities are presented which are driven by the steric mismatch between the individual reagents of these multicomponent reagents. Thus the LiTMP/GaR3 combination, which on its own fails to form a co-complex, functions as a highly regioselective base (LiTMP)-trap (GaR3) partnership for metalation of N-heterocycles such as diazines, 1,3 benzo-azoles and 2-picoline in a trans-metal-trapping (TMT) process that stabilizes the emerging sensitive carbanions. Taking advantage of related steric incompatibility, a novel monometallic FLP system pairing GaR3 with ItBu has been developed for activation of carbonyl compounds (via C=O insertion) and other molecules with acidic hydrogen atoms such as phenol and phenylacetylene. Shedding new light on how these non-cocomplexing partnerships operate and showcasing the potential of Ga reagents to engage in metalation reactions or FLP activations, areas where the use of this Group 13 metal is scant, this Forum Article aims to stimulate more interest and activity towards the advancement of organogallium chemistry

Synthetic and reactivity studies of hetero-tri-anionic sodium zincates

The synthesis and characterisation of several sodium zincate complexes is reported. The all-alkyl monomeric sodium zincate (PMEDTA)·Na(μ-CH2SiMe3)ZntBu2 2, is prepared by combining an equimolar quantity of tBu2Zn, nBuNa and PMDETA (N,N,N′,N′′,N′′-pentamethyldiethylenetriamine)]. A similar approach was used to prepare and isolate the unusual dimeric zincate [(PMEDTA)·Na(μ-nBu)ZntBu2]2 3. When an equimolar mixture of nBuNa, tBu2Zn and TMP(H) (2,2,6,6-tetramethylpiperidine) are combined in hexane, the hetero-tri-leptic TMP(H)-solvated zincate (TMPH)Na(μ-TMP)(μ-nBu)ZntBu 4 was forthcoming. Complex 4 can also be prepared using a rational approach [i.e., utilising two molar equivalents of TMP(H)]. When TMEDA is reacted with an equimolar mixture of nBuNa, tBu2Zn and TMP(H), the monomeric sodium zincate (TMEDA)Na(μ-TMP)(μ-nBu)ZntBu 5 was obtained – this complex is structurally similar to the synthetically useful relation TMEDA)·Na(μ-TMP)(μ-tBu)Zn(tBu) 1. By changing the sodium reagent used in the synthesis of 5, it was possible to prepare (TMEDA)Na(μ-TMP)(μ-Me3SiCH2)ZntBu 6. By reacting 5 with cis-DMP(H) (cis-2,6-dimethylpiperidine), the zincate could thermodynamically function as a amide base, to give the transamination product (TMEDA)Na(μ-cis-DMP)(μ-nBu)ZntBu 7, although no crystals could be grown. However, when HMDS(H) (1,1,1,3,3,3-hexamethyldisilazane) or PEA(H) [(+)-bis[(R)-1-phenylethyl]amine] is reacted with 5, crystalline (TMEDA)Na(μ-HMDS)(μ-nBu)ZntBu 8 or (TMEDA)Na(μ-PEA)(μ-nBu)ZntBu 9 are isolated respectively. With PNA(H) (N-phenylnaphthalen-1-amine) the reaction took a different course and resulted in the formation of the dimeric sodium amide complex [(TMEDA)Na(PNA)]2 10. When reacted with benzene, it appears that a TMEDA-free variant of 5 functions thermodyanically as an nBu base to yield the previously reported (TMEDA)Na(μ-TMP)(tBu)Zn(μ-C6H4)Zn(tBu)(μ-TMP)Na(TMEDA) 11. Finally when reacted with TEMPO (2,2,6,6-tetramethylpiperidinyloxy), 5 undergoes a single electron transfer reaction to form (TMEDA)Na(μ-TMP)(μ-TEMPO)ZnnBu 12

Multistep self-assembly of heteroleptic magnesium and sodium-magnesium benzamidinate complexes

Reaction of the magnesium bis-alkyl Mg(CH2SiMe3)(2) and the sodium amide NaHMDS (where HMDS = N(SiMe3)(2)) with benzonitrile yields the homometallic heteroleptic complex [PhC(NSiMe3)(2)Mg{mu-NC(CH2SiMe3)Ph}](2) (1). It appears that at least six independent reactions must have occurred in this one-pot reaction to arrive at this mixed benzamidinate ketimido product. Two benzonitrile solvated derivatives of Mg(CH2SiMe3)(2) (5a and 5b) have been synthesized, with 5a crystallographically characterized as a centrosymmetric (MgC)(2) cyclodimer. When, the components of 5a are allowed to react for longer, partial addition of the Mg-alkyl unit across the C N triple bond occurs to yield the trimeric species (Me3SiCH2)(2)Mg-3[mu-N=C(CH2SiMe3)Ph](4)center dot 2N CPh (6), with bridging ketimido groups and terminal alkyl groups. Finally, using the same starting materials as that which produced 1, but altering their order of addition, a magnesium bis-alkyl unit is inserted into the Na-N bonds of a benzamidinate species to yield a new sodium magnesiate complex, PhC(NSiMe3)(2)Mg(mu-CH2SiMe3)(2)Na center dot 2TMEDA (7). The formation of 7 represents a novel (insertion) route to mixed-metal species of this kind and is the first Such example to contain a bidentate terminal anion attached to the divalent metal center. All new species are characterized by H-1 and C-13 NMR spectroscopy and where appropriate by IR spectroscopy. The solid-state structures of complexes 1, 5a, and 7 have also been determined and are disclosed within

4-Formyl-2-nitrophenyl 3-nitro-2-methylbenzoate

In the title formyl nitro aryl benzoate derivative, CH NO, the benzene rings form a dihedral angle of 4.96(3)°. The mean plane of the central ester group, C-O-C-(=O)-C (r.m.s. deviation = 0.0484Å), is twisted away from the formyl nitro aryl and benzoate rings by 46.61(5) and 49.93(5)°, respectively. In the crystal, the molecules are packed forming C-H⋯O interactions in chains which propagate along [010]. Edge-fused R 3(15) rings are generated along this direction

The hydrochloride and hydrobromide salt forms of (S)-amphetamine

(S)-Amphetamine hydrochloride, C9H14ClN, has a Z′ = 6 structure with six independent cation, anion pairs. That these are indeed crystallographically independent is supported by different packing orientations of the cations and by observation of a wide range of cation conformations generated by rotation about the phenyl–CH2 bond. The supramolecular contacts about the anions also differ such that both a wide variation in the geometry of the three N–H···Cl hydrogen bonds formed by each chloride anion and differences in C–H···Cl contacts are apparent. (S)-Amphetamine hydrobromide, C9H14BrN, is broadly similar to the chloride in terms of cation conformation, the existance of three N–H···X hydrogen bond contacts per anion and the overall 2 dimensional hydrogen bonded sheet motif. However, only the chloride structure features organic bilayers and Z′ > 1

Mixed Ca/Sr salt forms of salicylic acid, tuning structure and aqueous solubility

Ten isostructural single-crystal diffraction studies of mixed cation Ca/Sr salt forms of the salicylate anion are presented, [Ca(1 − x)Srx(C7H5O3)2(OH2)2], where x = 0, 0.041, 0.083, 0.165, 0.306, 0.529, 0.632, 0.789, 0.835 and 1. The structure of an isostructural Sr/Ba species [Sr0.729Ba0.271(C7H5O3)2(OH2)2], is also described. The Ca/Sr structures form a series where, with increasing Sr content, the unit cell expands in both the crystallographic a and c directions (by 1.80 and 3.18% respectively), but contracts slightly in the b direction (−0.31%). The largest percentage structural expansion lies parallel to the direction of propagation of the one-dimensional coordination polymer that is the primary structural feature. This structural expansion is thus associated with increased M—O distances. Aqueous solubility measurements show that solubility generally increases with increasing Sr content·Thus tuning the composition of these mixed counterion salt forms leads to sytematic structural changes and allows solubility to be tuned to values between those for the pure Ca and Sr species