Effective or predatory funding? Evaluating the hidden costs of grant applications.

Researchers are spending an increasing fraction of their time on applying for funding; however, the current funding system has considerable deficiencies in reliably evaluating the merit of research proposals, despite extensive efforts on the sides of applicants, grant reviewers and decision committees. For some funding schemes, the systemic costs of the application process as a whole can even outweigh the granted resources-a phenomenon that could be considered as predatory funding. We present five recommendations to remedy this unsatisfactory situation.

Anion-Dependent Reactivity of Mono- and Dinuclear Boron Cations.

The dinuclear bis(N-heterocyclic carbene) borane adduct 2 rapidly reacts with tritylium salts at room temperature but the outcome is strongly impacted by the respective counter-ion. Using tritylium tetrakis(perfluoro-tert-butoxy)aluminate affords - depending on the solvent - either the bis(boronium) ion 4 or the hydride-bridged dication 5. In case of tritylium hexafluorophosphate, however, H/F exchange occurs between boron and phosphorus yielding the dinuclear BF3 adduct 3 along with phosphorus dihydride trifluoride. H/F exchange also takes place when using the mononuclear N-heterocyclic carbene BH3 adduct 6 and hence provides a facile route to PH2 F3 , which is usually synthesized in more complex reaction sequences regularly involving toxic hydrogen fluoride. DFT calculations shed light on the H/F exchange between the borenium ion and the [PF6 ]- counter-ion and the computed mechanism features only small barriers in line with the experimental observations.

A Planar Five-Membered Aromatic Ring Stabilized by Only Two π-Electrons.

Many chemicals known today are partially or fully aromatic, since a ring framework experiences additional stabilization through the delocalization of π-electrons. While aromatic rings with equal numbers of π-electrons and ring atoms such as benzene are particularly stable, those with the minimally required two π-electrons are very rare and yet remain limited to three- and four-membered rings if not stabilized in the coordination sphere of heavy metals. Here we report the facile synthesis of a dipotassium cyclopentagallene, a unique example of a five-membered aromatic ring stabilized by only two π-electrons. Single-crystal X-ray diffraction revealed a planar Ga5 ring with almost equal gallium-gallium bond lengths, which together with computational and spectroscopic data confirm its aromatic character. Our results prove that aromatic stabilization goes far beyond what has previously been assumed as minimum π-electron count in a five-atom ring fragment.

A Highly Fluorescent Dinuclear Aluminium Complex with Near-Unity Quantum Yield.

The high natural abundance of aluminium makes the respective fluorophores attractive for various optical applications, but photoluminescence quantum yields above 0.7 have yet not been reported for solutions of aluminium complexes. In this contribution, a dinuclear aluminium(III) complex featuring enhanced photoluminescence properties is described. Its facile one-pot synthesis originates from a readily available precursor and trimethyl aluminium. In solution, the complex exhibits an unprecedented photoluminescence quantum yield near unity (Φabsolute 1.0±0.1) and an excited-state lifetime of 2.3 ns. In the solid state, J-aggregation and aggregation-caused quenching are noted, but still quantum yields of 0.6 are observed. Embedding the complex in electrospun non-woven fabrics yields a highly fluorescent fleece possessing a quantum yield of 0.9±0.04.

Cooperative Bond Activation by a Bimetallic Main-Group Complex.

Inspired by natural metalloenzymes that efficiently catalyze a variety of transformations, chemists have developed large numbers of dinuclear transition-metal complexes with extraordinary properties and reactivity patterns. For main-group element compounds, however, metal-metal cooperativity is much less explored. Here we present the synthesis and characterization of a room-temperature-stable compound with two separated two-coordinated gallium(I) centers possessing both a lone pair of electrons and a vacant orbital, reminiscent of singlet carbenes. This species displays enhanced reactivity compared to its mononuclear counterpart due to bimetallic cooperativity that allows for the facile activation of strong C-F bonds across the gallium-gallium bond. Two mechanistic scenarios of the cooperative bond activation have been identified by DFT and DLPNO-CCSD(T) calculations.

Calcium and Magnesium Bis(ß-diketiminate) Complexes: Impact of the Alkylene Bridge on Schlenk-Type Rearrangements.

Dinuclear heteroleptic alkaline-earth-metal complexes are interesting synthetic targets because the close proximity of two metals allows for cooperative effects. However, these complexes are also prone to undergoing Schlenk-type rearrangements, affording less-active homoleptic complexes. Here we present the metalation of bis(ß-diketimine) ligands possessing flexible bridging groups, i.e., 1,2-ethylene, 1,3-propylene, and trans-1,2-cyclohexylene, using calcium and magnesium precursors. Four mononuclear homoleptic calcium complexes were obtained, highlighting the pronounced tendency of calcium to undergo Schlenk-like redistributions. In the case of magnesium, however, the bridging group plays a crucial role, yielding seven dinuclear heteroleptic complexes but also one mononuclear and one dinuclear homoleptic complexes. In addition, a trinuclear mixed heteroleptic-homoleptic magnesium complex, which is a rare example of an intermediate of the Schlenk equilibrium, was isolated.

Ligands with Two Monoanionic N,N-Binding Sites: Synthesis and Coordination Chemistry.

Polytopic ligands have become ubiquitous in coordination chemistry because they grant access to a variety of mono- and polynuclear complexes of transition metals as well as rare-earth and main-group elements. Nitrogen-based ditopic ligands, in which two monoanionic N,N-binding sites are framed within one molecule, are of particular importance and are therefore the primary focus of this review. In detail, bis(amidine)s, bis(guanidine)s, bis(ß-diimine)s, bis(aminotroponimine)s, bis(pyrrolimine)s, and miscellaneous bis(N,N-chelating) ligands are reviewed. In addition to the general synthetic protocols, the application of these ligands is discussed along with their coordination chemistry, the multifarious binding modes, and the ability of these ligands to bridge two (or more) metal(loids).

Synthesis and Coordination Chemistry of 3,4-Ethylene-Bridged 1,1,2,5-Tetrasubstituted Biguanides.

The synthesis of 3,4-ethylene-bridged 1,1,2,5-tetrasubstituted biguanides is reported, which are accessible by three alternative routes. Exemplary molecular structures of the ligand and an observed side product have been elucidated by X-ray diffraction analysis. Mono- and dinuclear complexes of the biguanide in both its neutral and monoanionic forms were obtained, including examples of aluminum, copper, magnesium, potassium, tin, and zinc, indicating a versatile coordination behavior, as evidenced by means of single-crystal X-ray diffraction analysis.

Nucleophilic Magnesium Silanide and Silaamidinate Derivatives.

Density functional theory (DFT) calculations demonstrate that the previously reported reaction of [(BDI)Mg-n-Bu] (BDI = HC{(Me)CN-Dipp}2; Dipp = 2,6-diisopropylphenyl) with the silaborane Me2PhSi-Bpin provides the magnesium silanide derivative [(BDI)MgSiMe2Ph], through the intermediacy of a short-lived silyl-pinacolato-organoborate species. The nucleophilic character of the resultant silanide anion is assayed through a series of reactions with RN═C═NR (R = i-Pr, Cy, t-Bu) and p-tolN═C═N-p-tol. When they are performed in a strict 1:1 stoichiometry, all four reactions result in silyl addition to the carbodiimide carbon center and formation of the corresponding ß-diketiminato magnesium silaamidinate complexes. Although the performance of the reaction of [(BDI)MgSiMe2Ph] with 2 equiv of p-tolylcarbodiimide also results in the formation of a silaamidinate anion, the second equivalent is observed to engage with the nucleophilic γ-methine carbon of the BDI ligand to provide a tripodal diimino-iminoamidate ligand. This behavior is judged to be a consequence of the enhanced electrophilicity of the N-aryl-substituted carbodiimide reagent, a viewpoint supported by a further reaction with the N-isopropyl silaamidinate complex [(BDI)Mg(i-PrN)2CSiMe2Ph]. This latter reaction not only provides an identical diimino-iminoamidate ligand but also results in 2-fold insertion of p-tolN═C═N-p-tol into a Mg-N bond between the magnesium center and the silaamidinate anion.

Dinuclear Aluminum Halide Complexes Based on Bis(ß-diketiminate) Ligands: Synthesis, Structures, and Electrochemical Characterization.

Twenty-three dinuclear aluminum halide complexes based on bis(ß-diketiminate) ligands with various flexible and rigid bridging groups have been synthesized and fully characterized by NMR and IR spectroscopy, cyclic voltammetry, and elemental analysis. In addition, nine complexes were structurally characterized by means of single-crystal X-ray diffraction. Attempts to reduce the dinuclear species using C8K remained unsuccessful, but the reduction potentials investigated by cyclic voltammetry indicate the principle feasibility.

Speech-Language Clinicians Working with Deaf Children: A Qualitative Study in Context.

Students who are deaf or hard of hearing (DHH) increasingly attend local public schools, in which speech and language clinicians (SLCs) may lack experience with the individualized needs of a heterogeneous student population. This study explored the experiences of SLCs with students who are DHH in three different types of educational settings. Fourteen SLCs were interviewed and discussed a case study. Responses were transcribed, data coded, and emergent themes identified. Analysis was verified through triangulation of data and trustworthiness strategies. Results indicated that the skill sets of SLCs working with children who were DHH were dependent on contextual factors, such as educational placement and communication mode used, and that development of these skills requires direct experience, collaboration, and structural supports. Institutions across the deaf education spectrum should consider forming alliances to improve information-sharing and collaborative learning in order to improve service delivery in all settings.

En Route to Bis-Carbene Analogues of the Heavier Group†13 Elements: Consideration of Bridging Group and Metal(I) Source.

With the aim of exploring the effect of steric constraints imposed on the metal-metal interaction of bis-carbene analogues of thallium by the linking scaffold, seven dinuclear thallium diyls with a series of rigid, semirigid, and flexible bridging scaffolds were synthesized. The solid-state molecular structures were determined for four of these compounds by single-crystal XRD and compared with the results of DFT calculations, which were performed for all substances. These compounds serve as models to investigate the metal-metal distance in the absence of co-coordinated molecules (additional ligands, solvent molecules). In addition, the effect of the metal(I) precursor, and more specifically the counterion, on the synthetic access to bis-carbene analogues of indium and thallium was investigated. For indium, only InI yields the desired dinuclear indium diyl. With InBr no reaction was observed, and using InCl gave rise to a mononuclear indium(III) compound. For thallium, both TlI and TlBr allow access to the related bis-carbene analogue, although the yield with the latter is significantly lower. In contrast, no reactions were observed with TlCl and TlBF4 .

One-, two-, and three-electron reduction of a cyclic alkyl(amino)carbene-SbCl3 adduct.

A cyclic alkyl(amino)carbene readily reacts with SbCl3 to form the corresponding Sb(III) adduct. One-electron reduction gives rise to the first example of a neutral antimony-centered radical characterized in solution. Two-electron reduction affords a Lewis base stabilized chloro-stibinidene, whereas three-electron reduction gives an antimony diatomic species capped by two carbenes. The radical has been characterized by EPR spectroscopy, while the structure of the other three species has been ascertained by single-crystal X-ray diffraction. In these four species, the formal oxidation state of the metalloid diminishes from III, to II, to I, and finally 0.

Metal-metal cooperativity boosts Lewis basicity and reduction properties of the bis(gallanediyl) CyL2Ga2.

The interplay of two proximate gallium centres equips the bimetallic complex CyL2Ga2 (1, CyL2 = 1,2-trans-Cy[NC(Me)C(H)C(Me)N(Dip)]2, Dip = 2,6-i-Pr2C6H3) with increased Lewis basicity and higher reducing power compared to the monometallic gallanediyl LGa (2, L = HC[MeCN(Dip)]2) as evidenced by cross-over experiments. Quantum chemical calculations were employed to support the experimental findings.

Novel triphenyltin(IV) compounds with carboxylato N-functionalized 2-quinolones as promising potential anticancer drug candidates: in vitro and in vivo evaluation.

Three newly synthesized triphenyltin(IV) compounds, Ph3SnL1 (L1- = 3-(4-methyl-2-oxoquinolin-1(2H)-yl)propanoato), Ph3SnL2 (L2- = 2-(4-methyl-2-oxoquinolin-1(2H)-yl)ethanoato), and Ph3SnL3 (L3- = 2-(4-hydroxy-2-oxoquinolin-1(2H)-yl)ethanoato), were characterized by elemental microanalysis, FT-IR spectroscopy and multinuclear (1H, 13C and 119Sn) NMR spectroscopy. A single X-ray diffraction study indicates that compounds Ph3SnL1 and Ph3SnL2 exhibit a 1D zig-zag chain polymeric structure, which in the case of Ph3SnL2 is additionally stabilized by π-interactions. In addition, the synthesized compounds were further examined using density functional theory and natural bond orbital analysis. The compounds have been evaluated for their in vitro anticancer activity against three human cell lines: MCF-7 (breast adenocarcinoma), A375 (melanoma), HCT116 (colorectal carcinoma), and three murine cell lines: 4T1 (breast carcinoma), B16 (melanoma), CT26 (colon carcinoma) using MTT and CV assays. The IC50 values fall in the nanomolar range, indicating that these compounds possess better anticancer activity than cisplatin. The study of the effect of the newly developed drug Ph3SnL1 showed its plasticity in achieving an antitumor effect in vitro, which depends on the specificity of the phenotype and the redox status of the malignant cell line and ranges from the initiation of apoptotic cell death to the induction of differentiation to a more mature cell form. In the syngeneic model of murine melanoma, Ph3SnL1 showed the potential to reduce the tumor volume similar to cisplatin, but in a well-tolerated form and with low systemic toxicity, representing a significant advantage over the conventional drug.

Isomer-selective thermal activation of methane in the gas phase by [HMO]+ and [M(OH)]+ (M=Ti and V).

Methane scrabble: To have the right elements is sometimes just not sufficient, as shown by [M(OH)](+) (M=Ti, V), which do not react with methane. However, reshuffling of the "tiles" to [HMO](+) changes the reactions behavior completely, leading to the first example of C-H bond activation of methane by an early first-row transition-metal cation.

A molecular aluminium fulleride.

The reaction of alumylene [(Dippnacnac)Al] (1) with C60 fashions the first example of a structurally characterised aluminium-fulleride complex, [{(Dippnacnac)Al}3C60] (2), in which the Al centres are covalently bound to significantly elongated 6 : 6 bonds. Hydrolysis of 2 yields C60H6 and the reaction of 2 with [{Mesnacnac)Mg}2] cleaved off the Al fragments by affording the fulleride [{Mesnacnac)Mg}6C60].

A tetranuclear magnesium hydride cluster with a four-coordinate hydride in near square-planar geometry.

A tetranuclear magnesium hydride complex based on the ß-oxo-δ-diiminate (BODDI) ligand was isolated. In the solid state, the complex features three bridging µ2-hydrides and one unprecedented four-coordinate hydride in a nearly square-planar coordination environment. In the solid state, two different coordination polymers are observed depending on whether the axial or equatorial oxygen lone pairs of 1,4-dioxane are engaged in bonding to magnesium.

Mechanistic aspects and elementary steps of N-H bond activation of ammonia and C-N coupling induced by gas-phase ions: a combined experimental/computational exercise.

In the last decades, N-H bond activation of ammonia and C-N coupling processes have formed the focus of broad research activities. More recently, gas-phase experiments combined with computational studies have provided rather detailed insights into the mechanisms and the elementary steps of these two reaction types. Some of the multifarious observations made and results obtained for these two processes mediated by gaseous "bare" or ligated ions are outlined in this review article.

[1-Meth-oxy-3-(pyridin-2-yl)indolizin-2-yl](pyridin-2-yl)methanone.

Methyl-ation of [1-hy-droxy-3-(pyridin-2-yl)indolizin-2-yl](pyridin-2-yl)methanone was performed via metalation with potassium tert-butano-late in toluene and a subsequent metathesis reaction with methyl iodide yielded the yellow title compound, C(20)H(15)N(3)O(2). The substituents at the indolizine unit are twisted [the indolizine ring system makes dihedral angles of 34.67 (7) and 77.49 (5)°, respectively, with the pyridyl and pyridinoyl rings] with single bonds between the central unit and the attached pyridine ring [1.459 (3) Å] and the pyridinoyl group [1.483 (3) Å]. There are no classical hydrogen bonds in the crystal structure.