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Eight [CNN] pincer nickel NHC chlorides, [RCcarbeneNamidoR′2Namine–Ni–Cl] (R/R′2 = quinolinyl/nBu (3a), quinolinyl/Me (3b), quinolinyl/PhCH2 (3c), (CH2)4/nBu (5a), (CH2)4/iPr (5b), Me2/nBu (5c), Me2/iPr (5d), and Me2/PhCH2 (5e)), were prepared by the reactions of related asymmetric [CNN] NHC preligands with Ni(DME)Cl2via N–H bond activation. The molecular structures of complexes 3a, 3b and 5a were investigated using single crystal XRD. The catalytic experiments showed that the nickel complexes could catalyze the hydrosilylation of unsaturated compounds like aldehydes and ketones, and complex 3b was found to exhibit the best catalytic activity at 30 °C. Using NaBHEt3 as an additive, the catalytic activity of 3b was greatly improved. Furthermore, it was found that good to complete conversion of aldehydes could be achieved within 1.5 h at 30 °C after pre-reacting 3b and NaBHEt3 with silane for 0.5 h. The substrate ketones could be converted to alcohols in good yields by prolonging the reaction time to 2.5 h at 30 °C. It is worth mentioning that all eight [CNN] pincer nickel NHC chlorides are stable in air, and this is rare in nickel catalysts for hydrosilylation of aldehydes and ketones. Moreover, the substrate universality of the catalytic system is also very good, with good functional group tolerance. The molecular structures of complexes 3a, 3b and 5a were investigated using single crystal XRD and a possible reaction mechanism was proposed. [ABSTRACT FROM AUTHOR]

The hydrido silyl iron complex (o-Ph2PC6H4SiMe2)Fe(PMe3)3H (2) was obtained via the activation of the Si–H bond of the bidentate silyl ligand o-Ph2P(C6H4)SiMe2H (1) by Fe(PMe3)4. 2 showed good to excellent catalytic activity in both the reduction of aldehydes/ketones and the dehydration of benzamide. In addition, with complex 2 as a catalyst, α,β-unsaturated carbonyls could be selectively reduced to the corresponding α,β-unsaturated alcohols. The mechanisms of the formation of 2 and the catalytic dehydration process are proposed and partly experimentally verified. [ABSTRACT FROM AUTHOR]

Three novel iron dinitrogen hydrides, [FeH(iPr-PSiMeP)(N2)(PMe3)] (1), [FeH(iPr-PSiPhP)(N2)(PMe3)] (2), and [FeH(iPr-PSiPh)(N2)(PMe3)] (3), supported by a silyl ligand are synthesized for the first time by changing the electronic effect and steric hindrance of the ligands through the reaction of ligands L1–L3 with Fe(PMe3)4 in a nitrogen atmosphere. The ligands containing an electron-donating group with large steric hindrance on the phosphorus atom are beneficial for the formation of dinitrogen complexes. A penta-coordinate iron hydride [FeH(iPr-PSiPh)(PMe3)2] (4) was formed through the reaction of ligand L3 with Fe(PMe3)4 in an argon atmosphere under the same conditions. The reactions between complexes 1–3 with an atmospheric pressure of dihydrogen gas resulted in Fe(II) dihydrides, [(iPr-PSiMe(μ-H)P)Fe(H)2(PMe3)] (5), [(iPr-PSiPh(μ-H)P)Fe(H)2(PMe3)] (6) and [(iPr-PSiPh(μ-H))Fe(H)2(PMe3)2] (7), with an η2-(Si–H) coordination. The isolation of dihydrides 5–7 demonstrates the ability of the dinitrogen complexes 1–3 to realize the activation of dihydrogen under ambient temperature and pressure. The molecular structures of complexes 1–7 were elucidated by single crystal X-ray diffraction analysis. The iron dinitrogen hydrides 1–3 are effective catalysts for the silylation of dinitrogen under ambient conditions and among them 3 is the best catalyst. [ABSTRACT FROM AUTHOR]

In this study, two [PCP] pincer silylene cobalt(I) complexes [((Ph2POCH2)2CH)Co(PMe3)(SiCl((NtBu)2CAr))] (Ar = Ph (2) and 4-MePh (3)) were synthesized through the substitution reaction of the [PCP] pincer cobalt(I) complex [((Ph2POCH2)2CH)Co(PMe3)2] (1) with silylene ligands: SiCl((NtBu)2CAr) (Ar = Ph (L1) and 4-MePh (L2)). The reaction of complex 2 with CO afforded the carbonyl silylene cobalt(I) complex [((Ph2POCH2)2CH)Co(CO)(SiCl((NtBu)2CPh))] (4), while complex 2 reacted with CH3I to give rise to cobalt(II) iodide [((Ph2POCH2)2CH)Co(I)(PMe3)] (6). With a catalyst loading of 2 mol%, complex 6 displayed efficient catalytic activity for hydrosilylation of alkenes by using Ph2SiH2 as the hydrogen source under mild conditions. The molecular structures of complexes 2, 3, 4 and 6 were determined by single crystal X-ray diffraction analysis. [ABSTRACT FROM AUTHOR]

Five [PSiP]-pincer iron hydrides 1–5, [(2-Ph2PC6H4)2HSiFe(H)(PMe3)2 (1), (2-Ph2PC6H4)2MeSiFe(H)(PMe3)2 (2), (2-Ph2PC6H4)2PhSiFe(H)(PMe3)2 (3), (2-(iPr)2PC6H4)2HSiFe(H)(PMe3) (4), and (2-(iPr)2PC6H4)2MeSiFe(H)(PMe3)2 (5)], were used as catalysts to study the effects of pyridine N-oxide and the electronic properties of [PSiP]-ligands on the catalytic hydrosilylation of carbonyl compounds. It was proved for the first time that this catalytic process could be promoted with pyridine N-oxide as the initiator at 30 °C because the addition of pyridine N-oxide is beneficial for the formation of an unsaturated hydrido iron complex, which is the key intermediate in the catalytic mechanism. Complex 4 as the best catalyst shows excellent catalytic performance. Among the five complexes, complex 3 was new and the molecular structure of complex 3 was determined by single crystal X-ray diffraction. A proposed mechanism was discussed. [ABSTRACT FROM AUTHOR]

Four NHC [CNN] pincer nickel (II) complexes, [iPrCNN (CH2)4‐Ni‐Br] (5a), [nBuCNN (CH2)4‐Ni‐Br] (5b), [iPrCNN (Me)2‐Ni‐Br] (6a) and [nBuCNN (Me)2‐Ni‐Br] (6b), bearing unsymmetrical [C (carbene)N (amino)N (amine)] ligands were synthesized by the reactions of [CNN] pincer ligand precursors 4 with Ni (DME)Cl2 in the presence of Et3N. Complexes 5a and 5b are new and were completely characterized. The transfer hydrogenation of ketones catalyzed by the four pincer nickel complexes were explored. Complexes 5a and 6a have better catalytic activity than 5b and 6b. With a combination of NaOtBu/iPrOH/80 °C and 2% catalyst loading of 5a, 77–98% yields of aromatic alcohols could be obtained. [ABSTRACT FROM AUTHOR]

Polyfluorinated aryl imines 2,4,5-R1,R2,R3-C6H2-HC=N-1-C10H7 (R1 = F, R2 = F, R3 = H (1); R1 = F, R2 = H, R3 = F (2) and R1 = F, R2 = F, R3 = F (3)) and F5C6-HC=N-1-C10H7 (7) reacted with CoMe(PMe3)4 to give rise to hydrido [CNC]-pincer cobalt(iii) complexes (2,4,5-R1,R2,R3-C6H-HC=N-1-C10H6)Co(H)(PMe3)2 (R1 = F, R2 = F, R3 = H (4); R1 = F, R2 = H, R3 = F (5); R1 = F, R2 = F, R3 = F (6)) and (F4C6-HC=N-1-C10H6)Co(H)(PMe3)2 (8) via selective C–F/C–H bond activation. Penta-coordinate dicarbonyl cobalt(i) complexes (2,4,5-R1,R2,R3-C6H-HC=N-1-C10H7)Co(CO)2(PMe3) (R1 = F, R2 = H, R3 = F (9); R1 = F, R2 = F, R3 = F (10)) were obtained from reactions of hexa-coordinate cobalt(iii) complexes 5 and 6 with carbon monoxide through reductive elimination. Cobalt(iii) halides (2,4,5-R1,R2,R3-C6H-HC=N-1-C10H6)Co(i)(PMe3)2 (R1 = F, R2 = F, R3 = H (11); R1 = F, R2 = H, R3 = F (12); R1 = F, R2 = F, R3 = F (13)) and (2,4,5-R1,R2,R3-C6H-HC=N-1-C10H6)Co(Br)(PMe3)2 (R1 = F, R2 = F, R3 = H (14); R1 = F, R2 = H, R3 = F (15); R1 = F, R2 = F, R3 = F (16)) were prepared by the interaction between hydrido cobalt(iii) complexes 4–6 and MeI or EtBr. The molecular configurations of complexes 4, 8, and 11 were determined by single crystal X-ray diffraction. We then confirmed that the four hydrido cobalt(iii) complexes 4–6 and 8 could be used as catalysts for reduction of aldehydes and ketones. Complex 8 is the best catalyst among the four complexes and can selectively catalyze the carbonyl groups of α,β-unsaturated aldehydes and ketones. [ABSTRACT FROM AUTHOR]

Two novel cobalt Schiff base complexes 3 and 4, ((2-PPh2)C6H4)C=N(C10H7)Co(PMe3)2 (3) and ((2-PPh2)C6H4)CH=N(C6H5)Co(PMe3)2 (4) with η2(C–H) coordination, were synthesized by the reactions of Schiff base preligands ((2-PPh2)C6H4)CH=N(C10H7) (1) and ((2-PPh2)C6H4)CH=N(C6H5) (2) with CoMe(PMe3)4via sp2 C–H bond activation. Under similar reaction conditions, the reactions of Co(PMe3)4 with 1 and 2 gave rise to the simple π-(C=N)-coordinated cobalt(0) complexes ((2-PPh2)C6H4)CH=N(C10H7)Co(PMe3)2 (5) and ((2-PPh2)C6H4)CH=N(C6H5)Co(PMe3)2 (6). Complex ((2-PPh2)C6H4)C=N(C10H6)CoI(PMe3)2 (7) was obtained through the reaction of 3 with iodomethane via the activation of the second C–H bond in 1. The substitution reaction of complex 3 with carbon monoxide afforded the dicarbonyl cobalt(i) complex ((2-PPh2)C6H4)C=N(C10H7)Co(CO)2(PMe3) (8). The molecular structures of 4, 5, 7 and 8 were determined by single-crystal X-ray diffraction. [ABSTRACT FROM AUTHOR]

Correction for 'Pyridine N-oxide promoted hydrosilylation of carbonyl compounds catalyzed by [PSiP]-pincer iron hydrides' by Guoliang Chang et al., Dalton Trans., 2020, 49, 9349–9354, DOI: 10.1039/D0DT00392A. [ABSTRACT FROM AUTHOR]

A series of phosphorus‐chalcogen chelated hydrido iron (II) complexes 1–7, (o‐(R'2P)‐p‐R‐C6H4Y)FeH (PMe3)3 (1: R = H, R' = Ph, Y = O; 2: R = Me, R' = Ph, Y = O; 3: R = H, R' = iPr, Y = O; 4: R = Me, R' = iPr, Y = O; 5: R = H, R' = Ph, Y = S; 6: R = Me, R' = Ph, Y = S; 7: R = H, R' = Ph, Y = Se), were synthesized. The catalytic performances of 1–7 for dehydration of amides to nitriles were explored by comparing three factors: (1) different chalcogen coordination atoms Y; (2) R' group of the phosphine moiety; (3) R substituent group at the phenyl ring. It is confirmed that 5 with S as coordination atom has the best catalytic activity and 7 with Se as coordination atom has the poorest catalytic activity among complexes 1, 5 and 7. Electron‐rich complex 4 is the best catalyst among the seven complexes and the dehydration reaction was completed by using 2 mol% catalyst loading at 60 °C with 24 hr in the presence of (EtO)3SiH in THF. Catalyst 4 has good tolerance to many functional groups. Among the seven iron complexes, new complexes 3 and 4 were obtained via the O‐H bond activation of the preligands o‐iPr2P(C6H4)OH and o‐iPr2P‐p‐Me‐(C6H4)OH by Fe(PMe3)4. Both 3 and 4 were characterized by spectroscopic methods and X‐ray diffraction analysis. The catalytic mechanism was experimentally studied and also proposed. [ABSTRACT FROM AUTHOR]