Dinitrogen Complexes of Sulfur-Ligated Iron

We report a unique class of dinitrogen complexes of iron featuring sulfur donors in the ancillary ligand. The ligands utilized are related to the recently studied tris(phosphino)silyl ligands (2-R_2PC_6H_4)_3Si (R = Ph, iPr) but have one or two phosphine arms replaced with thioether donors. Depending on the number of phosphine arms replaced, both mononuclear and dinuclear iron complexes with dinitrogen are accessible. These complexes contribute to a desirable class of model complexes that possess both dinitrogen and sulfur ligands in the immediate iron coordination sphere

Coordination polymers and isomerism; a study using silver(I) and a ∏-stacked ligand

The ligand 2,5-bis(2-pyridylmethylsulfanylmethyl)pyrazine (L) was prepared by the base coupling of 2-(sulfanylmethyl)pyridine and 2,5-bis(chloromethyl)pyrazine. This new ligand was treated with AgClO₄ in a 1 1 metal-to-ligand ratio and with AgNO₃in a 2 1 metal-to-ligand ratio to give coordination polymers. The crystal structures of {[Ag(L)]ClO₄}∞ ( 1) and {[Ag₂(L)](NO₃)₂}∞ ( 2) were determined. The Ag(I) ions in the one-dimensional polymeric chains of 1 adopted square-pyramidal geometries with the pyridine and pyrazine N donors coordinated in an extremely bent fashion. The structure of 2 revealed two isomeric polymer chains in the one crystal forming a single supramolecular array. The isomeric polymers differed in the donor atoms about the Ag(I) ions and in the arrangement of adjacent ligands along the chain. A feature of both structures was that L adopted a three-layer ∏-stacked arrangement

Silver selective electrodes based on thioether functionalized calix[4]arenes as ionophores

Silver selective electrodes based on thioether functionalized calix[4]arenes 1 and 2 as ionophores were investigated. For both ionophores the selectivity coefficients (log kAg,M) were lower than −2.2 for Hg(II) and lower than −4.6 for other cations tested. The best results were obtained with membranes containing dithioether functionalized calix[4]arene (ionophore 2), potassium tetrakis(4-chlorophenyl) borate (KTpCIPB) and bis(1-butylpentyl)adipate (BBPA) as a plasticizer. The Ag(I)-response functions exhibited almost theoretical Nernstian slopes in the activity range 10−6–10−1M of silver ions.\ud \u

A homoleptic phosphine adduct of Tl(I)

A homoleptic phosphine adduct of thallium(I) supported by a tris(phosphino)borate ligand has been isolated and structurally characterized

Investigating the Effects of Tethered, Axial Lewis Base Coordination on Rhodium(II) Paddlewheel Complexes

Dirhodium(II) paddlewheel complexes are highly renowned for their use in diazo decomposition to form a metallic-carbenoid species. This species has been used for a diverse range of chemical transformations including cyclopropanation, cycloproprenation, C-H functionalization, and X-H (Si, S, O, N) insertion reactions. Modulation of these catalysts traditionally involve the exchange of bridging ligands which have profound effects on the catalyst’s reactivity, chemo, and enantioselectivity. Recent interest has turned towards to modifying the axial sites present in the complex as an additional means of modulating catalytic activity. These sites normally serve as the active site of the catalyst, but coordination of Lewis Bases one of the sites are known to be beneficial to chemo and enantioselectivity. However, a main problem encountered in this field is the lack of control of coordination to axial site. This work aims to examine the development of novel ligands containing a pendant chain containing a Lewis base, and their incorporation into the rhodium(II) paddlewheel scaffold. Incorporation of these tether containing ligands allows for more direct control of the location of the Lewis base and effectively increasing the local concentration of the Lewis base near the active site. Ligands derived from amino acids that contained either a phosphite or a thioether moiety were synthesized and attempts to exchange onto the rhodium complex were investigated. Exchange of the phosphite containing ligands was unsuccessful due to problems with oxidation. The thioether ligands proved to be more robust in comparison with successful exchange on to the catalyst scaffold with a variety of thioether derivatives. Evaluation of these complexes in Si-H insertion and cyclopropanation reactions revealed that the presence of the tethered thioether does indeed provide a positive benefit, with increase yields as compared to a control with no tethered thioether additive

Toward Charge-neutral ‘soft scorpionates’: Coordination Chemistry and Lewis Acid Promoted Isomerization of tris(1-organo-imidazol-2-ylthio)methanes

Two tris(1-organo-imidazol-2-ylthio)methanes, HC(S-timR)3 (R = organo = methyl, tert-butyl), have been prepared by a triphasic reaction between chloroform, the appropriate heterocycle, and saturated aqueous solutions of Na2CO3, in the presence of a phase transfer agent, (NBu4)(Br). These ligands have been characterized both spectroscopically and by single crystal X-ray diffraction. The reaction chemistry of these potentially N,N,N-tripodal ligands with AgBF4 was also explored where simple 1:1 coordination complexes could be isolated from reactions performed in THF solution at room temperature. The derivative {Ag[HC(S-timMe)3]}(BF4) was structurally characterized which showed that the ligand binds in a μ–κ2N,κ1N-mode to give a coordination polymer with an interesting layered supramolecular structure. Surprisingly, heating CH3CN solutions of the silver complexes at reflux resulted in decomposition of the complex and concomitant isomerization of the ligands to give metal-free tris(3-organo-1-imidazole-2-thione)methane, HC(N-imtR)3; the heretofore elusive charge-neutral analogues of the well-studied ‘soft scorpionate’ TmR− anions. The solution isomerization of HC(S-timR)3 to HC(N-imtR)3 was found to be general, occurring in a variety of solvents with any of a host of different Lewis acids [para-toluenesulfonic acid, KPF6, and M(CO)5Br (M = Mn, Re)] but did not occur by heating in the absence of Lewis acid. The compound HC(N-imtMe)3 exhibited unusually low solubility in common organic solvents. Single crystal X-ray diffraction of HC(N-imtMe)3 revealed a remarkable honeycomb supramolecular structure with ca. 5 Å channels filled with solvent. The robust nature of this solid is a result of strong dipolar stacking interactions of molecules into polymer chains bolstered by concerted π–π and CH–π interactions involving the heterocycles, holding the chains together in the remaining two dimensions

Formation of gold colloids using thioether derivatives as stabilizing ligands

Thioethers were used as adsorbates for preparing gold nanoparticles. Different thioether derivatives having from 1 to 4 thioether functionalities were synthesized. Colloids were prepared in a two-phase system, and characterized by 1H NMR and transmission electron microscopy (TEM). The stability of colloids protected by thioethers increases with the number of ligands per molecule. Monothioethers need longer chain lengths or costabilization by (oct)4NBr in order to give stable, redispersible gold colloids. Gold colloids stabilized by the bis(thioether) 5 could not be redispersed after precipitation. Colloids stabilized by the tris(thioether) 6 were only formed at elevated temperature (60°C) indicating the need of chain reorientation for attaining stable colloids. Tris(thioether) 7 gave stable colloids at room temperature, which could be redispersed even after precipitation. Tetrakis(thioether) 8 gave the smallest particle size and narrowest size distributio

Tunable, Functional Diblock Copolypeptide Hydrogels Based on Methionine Homologs.

The preparation of new diblock copolypeptide hydrogels derived from homologs of l-methionine, that is, l-homomethionine and l-6-(methylthio)-l-norleucine is described. Compared to l-methionine residues, use of l-methionine homologs allow improved copolymerization with l-leucine residues to give well-defined block copolypeptides. These copolypeptides are subsequently modified using robust thioether alkylation reactions employing a variety of functional epoxides, which yield samples capable of forming transparent, self-healing hydrogels in water. The facile variation of different functional epoxides for postpolymerization modification is found to allow predictable functionalization and tuning of hydrogel properties by the modification of simple precursors