Bioinspired Diiron Complex with Proton Shuttling and Redox-Active Ligand for Electrocatalytic Hydrogen Evolution.

A µ-oxo diiron complex, featuring the pyridine-2,6-dicarboxamide-based thiazoline-derived redox-active ligand, H2L (H2L = N2,N6-bis(4,5-dihydrothiazol-2-yl)pyridine-2,6-dicarboxamide), was synthesized and thoroughly characterized. [FeIII-(µ-O)-FeIII] showed electrocatalytic hydrogen evolution reaction activity in the presence of different organic acids of varying pKa values in dimethylformamide. Through electrochemical analysis, we found that [FeIII-(µ-O)-FeIII] is a precatalyst that undergoes concerted two-electron reduction to generate an active catalyst. Fourier transform infrared spectrum of reduced species and density functional theory (DFT) investigation indicate that the active catalyst contains a bridged hydroxo unit which serves as a local proton source for the Fe(III) hydride intermediate to release H2. We propose that in this active catalyst, the thiazolinium moiety acts as a proton-transferring group. Additionally, under sufficiently strong acidic conditions, bridged oxygen gets protonated before two-electron reduction. In the presence of exogenous acids of varying strengths, it displays electro-assisted catalytic response at a distinct applied potential. Stepwise electron-transfer and protonation reactions on the metal center and the ligand were studied through DFT to understand the thermodynamically favorable pathways. An ECEC or EECC mechanism is proposed depending on the acid strength and applied potential.

Exploiting Coordination Behavior of 7-Azaindole for Mechanistic Investigation of Chan-Lam Coupling and Application to 7-Azaindole Based Pharmacophores.

Multiple spectroscopic techniques, along with single-crystal X-ray analysis, have been used to reveal the detailed structural and electronic information on reaction intermediates of a new copper(II)-DBU catalytic system for the N-arylation of 7-Azaindole. The reaction mixture of Chan-Lam cross-coupling yields two dimeric copper(II)-7-azaindole complexes, including one attached with DBU, prior to adding arylboronic acid and are confirmed structurally and spectroscopically. A suitable mechanism has been proposed using the dimeric copper(II) complex as a catalyst for the coupling reactions. The role of DBU as a base and also as an auxiliary ligand in the course of the reaction has been established. The transmetalated monomeric aryl-copper(II) species generated from the dimeric unit is oxidized by another equivalent of copper(II) to yield an aryl-copper(III) intermediate for facile N-arylation, which has been authenticated with UV-vis spectroscopy. The regeneration of the copper(II)-catalyst by aerial oxidation of colorless copper(I) species (generated via reductive elimination and disproportionation step) is confirmed by mass and absorption spectroscopy. Detailed DFT and TD-DFT calculations help to rationalize the proposed reaction intermediates and their corresponding electronic transitions. Moreover, the confirmation of copper(I)-7-azaindole intermediate via HRMS reaffirmed the involvement of Cu(II)/Cu(III)/Cu(I) species in the Chan-Lam type of coupling. A medicinally-important 7-azaindole-based SHP2 inhibitor has been synthesized via sequential arylation.

Carbonylative Transformations Using a DMAP-Based Pd-Catalyst through Ex Situ CO Generation.

A phosphine-free, efficient protocol for aminocarbonylation and carbonylative Suzuki-Miyaura coupling has been developed using a novel palladium complex, [PdII(DMAP)2(OAc)2]. The complex was successfully synthesized using a stoichiometric reaction between PdII(OAc)2 and DMAP in acetone at room temperature and characterized using single-crystal X-ray analysis. Only 5 mol % catalyst loading was sufficient for effective carbonylative transformations. "Chloroform-COware" chemistry was utilized for safe and facile insertion of the carbonyl unit using chloroform as an inexpensive CO source in a two-chamber setup. Various value-added pharmaceutically relevant compounds such as CX-516, CX-546, and farampator were synthesized using the technique. Furthermore, the commercially designed COware was engineered to COware-RB setup for sequential one-pot synthesis of indenoisoquinolines (topoisomerase I inhibitors).

Iron(III) Complexes of a Hexadentate Thioether-Appended 2-Aminophenol Ligand: Redox-Driven Spin State Switchover.

A green complex [Fe(L3)] (1), supported by the deprotonated form of a hexadentate noninnocent redox-active thioether-appended 2-aminophenolate ligand (H4L3 = N,N'-bis(2-hydroxy-3,5-di-tert-butylphenyl)-2,2'-diamino(diphenyldithio)ethane), has been synthesized and structurally characterized at 100(2) K and 298(2) K. In CH2Cl2, 1 displays two oxidative and a reductive one-electron redox processes at E1/2 values of -0.52 and 0.20 V, and -0.85 V versus the Fc+/Fc redox couple, respectively. The one-electron oxidized 1+ and one-electron reduced 1- forms, isolated as a blackish-blue solid 1(PF6)·CH2Cl2 (2) and a gray solid [Co(η5-C5H5)2]1·DMF (3), have been structurally characterized at 100(2) K. Structural parameters at 100 K of the ligand backbone and metrical oxidation state values unambiguously establish the electronic states as [FeIII{(LAPO,N)2-}{(LISQO,N)•-}{(LS,S)0}] (1) (two tridentate halves are electronically asymmetric-ligand mixed-valency), [FeIII{(LISQO,N)•-}{(LISQO,N)•-}{(LS,S)0}]+ (1+), and [FeIII{(LAPO,N)2-}{(LAPO,N)2-}{(LS,S)0}]- (1-) [dianionic 2-amidophenolate(2-) (LAPO,N)2- and monoanionic 2-iminobenzosemiquinonate(1-) π-radical (Srad = 1/2) (LISQ)•- redox level]. Mössbauer spectral data of 1 at 295, 200, and 80 K reveal that it has a major low-spin (ls)-Fe(III) and a minor ls-Fe(II) component (redox isomers), and at 7 K, the major component exists exclusively. Thus, in 1, the occurrence of a thermally driven valence-tautomeric (VT) equilibrium (asymmetric) [FeIII{(LAPO,N)2-}{(LISQO,N)•-}{(LS,S)0}] ⇌ (symmetric) [FeII{(LISQO,N)•-}{(LISQO,N)•-}{(LS,S)0}] (80-295 K) is implicated. Mössbauer spectral parameters unequivocally establish that 1+ is a ls-Fe(III) complex. In contrast, the monoanion 1- contains a high-spin (hs)-Fe(III) center (SFe = 5/2), as is deduced from its Mössbauer and EPR spectra. Complexes 1-3 possess total spin ground states St = 0, 1/2, and 5/2, respectively, based on 1H NMR and EPR spectra, the variable-temperature (2-300 K) magnetic behavior of 2, and the µeff value of 3 at 300 K. Broken-symmetry density functional theory (DFT) calculations at the B3LYP-level of theory reveal that the unpaired electron in 1+/2 is due to the (LISQ)•- redox level [ls-Fe(III) (SFe = 1/2) is strongly antiferromagnetically coupled to one of the (LISQ)•- radicals (Srad = 1/2)], and 1-/3 is a hs-Fe(III) complex, supported by (L3)4- with two-halves in the (LAP)2- redox level. Complex 1 can have either a symmetric or asymmetric electronic state. As per DFT calculation, the former state is stabilized by -3.9 kcal/mol over the latter (DFT usually stabilizes electronically symmetric structure). Time-dependent (TD)-DFT calculations shed light on the origin of observed UV-vis-NIR spectral absorptions for 1-3 and corroborate the results of spectroelectrochemical experiments (300-1100 nm) on 1 (CH2Cl2; 298 K). Variable-temperature (218-298 K; CH2Cl2) absorption spectral (400-1000 nm) studies on 1 justify the presence of VT equilibrium in the solution-state.

Phenoxazinyl Zn(II) diradical complex formed via redox-driven cyclization of a 2-aminophenol-based N3O ligand. Isolation of the modified N3 ligand radical and its Ni(II) complex.

Aerobic reaction between the pyridine-2-carboxamide-2-aminophenol N3O ligand (H3L1) and Zn(ClO4)2·6H2O in CH3CN affords an N3 phenoxazinylate coordinated Zn(II) complex; its diradical electronic structure [ZnII{(L1*)˙-}2] has been elucidated from redox, spectroscopic (UV-VIS and EPR), and magnetic measurements and DFT calculations. Isolation and characterization of the metal-assisted redox-driven modified N3 ligand as a radical cation (H2L1*)˙+ and its Ni(II)-diradical complex [NiII{(L1*)˙-}2] have also been achieved.

CuF2/DMAP-Catalyzed N-Vinylation: Scope and Mechanistic Study.

CuF2/DMAP has been established as an excellent catalytic system for vinylsilane-promoted N-vinylation of amides and azoles at room temperature without an external fluoride source. A mechanism has been proposed on the basis of the isolation of reactive intermediate [Cu(DMAP)4Cl2], fluoride ion-assisted transmetalation, and ultraviolet-visible spectroscopic studies. The catalytic efficiency of the synthesized and structurally characterized [Cu(DMAP)4Cl2] complex has been demonstrated. The valuable monomers for water-soluble polymers, viz., NVP, NVC, and NVIBA, were synthesized on a gram scale.

Ni(II) complexes of a new tetradentate NN'N''O picolinoyl-1,2-phenylenediamide-phenolate redox-active ligand at different redox levels.

Three square planar nickel(II) complexes of a new asymmetric tetradentate redox-active ligand H3L2 in its deprotonated form, at three redox levels, open-shell semiquinonate(1-) π radical, quinone(0) and closed-shell dianion of its 2-aminophenolate part, have been synthesized. The coordinated ligand provides N (pyridine) and N' and N'' (carboxamide and 1,2-phenylenediamide, respectively) and O (phenolate) donor sites. Cyclic voltammetry on the parent complex [Ni(L2)] 1 in CH2Cl2 established a three-membered electron-transfer series (oxidative response at E1/2 = 0.57 V and reductive response at -0.32 V vs. SCE) consisting of neutral, monocationic and monoanionic [Ni(L2)]z (z = 0, 1+ and 1-). Oxidation of 1 with AgSbF6 affords [Ni(L2)](SbF6) (2) and reduction of 1 with cobaltocene yields [Co(η5-C5H5)2][Ni(L2)] (3). The molecular structures of 1·CH3CN, 2·0.5CH2Cl2 and 3·C6H6 have been determined by X-ray crystallography at 100 K. Characterization by 1H NMR, X-band EPR (gav = 2.006 (solid); 2.008 (CH2Cl2-C6H5CH3 glass); 80 K) and UV-VIS-NIR spectral properties established that 1, 2 and 3 have [NiII{(L2)˙2-}], [NiII{(L2)-}]+/1+ and [NiII{(L2)3-}]-/1- electronic states, respectively. Thus, the redox processes are ligand-centred. While 1 possesses paramagnetic St (total spin) = 1/2, 2 and 3 possess diamagnetic ground-state St = 0. Interestingly, the variable-temperature (2-300 K) magnetic measurement reveals that 1 with the St = 1/2 ground state attains the antiferromagnetic St = 0 state at a very low temperature, due to weak noncovalent interactions via π-π stacking. Density functional theory (DFT) electronic structural calculations at the B3LYP level of theory rationalized the experimental results. In the UV-VIS-NIR spectra, broad absorptions are recorded for 1 and 2 in the range of 800-1600 nm; however, such an absorption is absent for 3. Time-dependent (TD)-DFT calculations provide a very good fit with the experimental spectra and allow us to identify the observed electronic transitions.

Assisted π-stacking: a strong synergy between weak interactions.

Synergy between a pair of weak non-covalent interactions can predispose a molecular self-assembly towards a specific pathway. We report assisted π-stacking, a synergy between aromatic π-stacking and n →π* interactions that exhibits an unprecedented strength and thermal stability. Natural bond orbital analysis reveals the non-additive nature of the interaction.