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1. N ₃ -Ligated nickel( ii ) diketonate complexes: synthesis, characterization and evaluation of O ₂ reactivity

   https://doi.org/10.1039/d0dt01338b  

   Elsberg, Josiah G.; Peterson, Austin; Fuller, Amy L.; Berreau, Lisa M. (January 2020, Dalton Transactions)

   Interest in O 2 -dependent aliphatic carbon–carbon (C–C) bond cleavage reactions of first row divalent metal diketonate complexes stems from the desire to further understand the reaction pathways of enzymes such as DKE1 and to extract information to develop applications in organic synthesis. A recent report of O 2 -dependent aliphatic C–C bond cleavage at ambient temperature in Ni( ii ) diketonate complexes supported by a tridentate nitrogen donor ligand [(MBBP)Ni(PhC(O)CHC(O)Ph)]Cl ( 7-Cl ; MBBP = 2,6-bis(1-methylbenzimidazol-2-yl)pyridine) in the presence of NEt 3 spurred our interest in further examining the chemistry of such complexes. A series of new TERPY-ligated Ni( ii ) diketonate complexes of the general formula [(TERPY)Ni(R 2 -1,3-diketonate)]ClO 4 ( 1 : R = CH 3 ; 2 : R = C(CH 3 ) 3 ; 3 : R = Ph) was prepared under air and characterized using single crystal X-ray crystallography, elemental analysis, 1 H NMR, ESI-MS, FTIR, and UV-vis. Analysis of the reaction mixtures in which these complexes were generated using 1 H NMR and ESI-MS revealed the presence of both the desired diketonate complex and the bis-TERPY derivative [(TERPY) 2 Ni](ClO 4 ) 2 ( 4 ). Through selective crystallization 1–3 were isolated in analytically pure form. Analysis of reaction mixtures leading to the formation of the MBBP analogs [(MBBP)Ni(R 2 -1,3-diketonate)]X (X = ClO 4 : 5 : R = CH 3 ; 6 : R = C(CH 3 ) 3 ; 7-ClO4 : R = Ph; X = Cl: 7-Cl : R = Ph) using 1 H NMR and ESI-MS revealed the presence of [(MBBP) 2 Ni](ClO 4 ) 2 ( 8 ). Analysis of aerobic acetonitrile solutions of analytically pure 1–3 , 5 and 6 containing NEt 3 and in some cases H 2 O using 1 H NMR and UV-vis revealed evidence for the formation of additional bis-ligand complexes ( 4 and 8 ) but suggested no oxidative diketonate cleavage reactivity. Analysis of the organic products generated from 3 , 7-ClO4 and 7-Cl revealed unaltered dibenzoylmethane. Our results therefore indicate that N 3 -ligated Ni( ii ) complexes of unsubstituted diketonate ligands do not exhibit O 2 -dependent aliphatic C–C bond clevage at room temperature, including in the presence of NEt 3 and/or H 2 O. 

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2. Characterization of paramagnetic states in an organometallic nickel hydrogen evolution electrocatalyst

   https://doi.org/10.1038/s41467-023-36609-7  

   Chakrabarti, Sagnik; Sinha, Soumalya; Tran, Giang N.; Na, Hanah; Mirica, Liviu M. (February 2023, Nature Communications)

   Abstract Significant progress has been made in the bioinorganic modeling of the paramagnetic states believed to be involved in the hydrogen redox chemistry catalyzed by [NiFe] hydrogenase. However, the characterization and isolation of intermediates involved in mononuclear Ni electrocatalysts which are reported to operate through a Ni^I/IIIcycle have largely remained elusive. Herein, we report a Ni^IIcomplex (NCHS2)Ni(OTf)2, where NCHS2 is 3,7-dithia-1(2,6)-pyridina-5(1,3)-benzenacyclooctaphane, that is an efficient electrocatalyst for the hydrogen evolution reaction (HER) with turnover frequencies of ~3,000 s⁻¹and a overpotential of 670 mV in the presence of trifluoroacetic acid. This electrocatalyst follows a hitherto unobserved HER mechanism involving C-H activation, which manifests as an inverse kinetic isotope effect for the overall hydrogen evolution reaction, and Ni^I/Ni^IIIintermediates, which have been characterized by EPR spectroscopy. We further validate the possibility of the involvement of Ni^IIIintermediates by the independent synthesis and characterization of organometallic Ni^IIIcomplexes. 

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3. Atomically Dispersed Single Ni Site Catalysts for Nitrogen Reduction toward Electrochemical Ammonia Synthesis Using N ₂ and H ₂ O

   https://doi.org/10.1002/smtd.201900821  

   Mukherjee, Shreya; Yang, Xiaoxuan; Shan, Weitao; Samarakoon, Widitha; Karakalos, Stavros; Cullen, David A.; More, Karren; Wang, Maoyu; Feng, Zhenxing; Wang, Guofeng; et al (February 2020, Small Methods)

   Abstract Ammonia (NH₃) electrosynthesis gains significant attention as NH₃is essentially important for fertilizer production and fuel utilization. However, electrochemical nitrogen reduction reaction (NRR) remains a great challenge because of low activity and poor selectivity. Herein, a new class of atomically dispersed Ni site electrocatalyst is reported, which exhibits the optimal NH₃yield of 115 µg cm⁻²h⁻¹at –0.8 V versus reversible hydrogen electrode (RHE) under neutral conditions. High faradic efficiency of 21 ± 1.9% is achieved at ‐0.2 V versus RHE under alkaline conditions, although the ammonia yield is lower. The Ni sites are stabilized with nitrogen, which is verified by advanced X‐ray absorption spectroscopy and electron microscopy. Density functional theory calculations provide insightful understanding on the possible structure of active sites, relevant reaction pathways, and confirm that the Ni‐N₃sites are responsible for the experimentally observed activity and selectivity. Extensive controls strongly suggest that the atomically dispersed NiN₃site‐rich catalyst provides more intrinsically active sites than those in N‐doped carbon, instead of possible environmental contamination. This work further indicates that single‐metal site catalysts with optimal nitrogen coordination is very promising for NRR and indeed improves the scaling relationship of transition metals. 

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4. The mechanism of directed Ni( ii )-catalyzed C–H iodination with molecular iodine

   https://doi.org/10.1039/C7SC04604A  

   Haines, Brandon E.; Yu, Jin-Quan; Musaev, Djamaladdin G. (January 2018, Chemical Science)

   The density functional theory method is used to elucidate the elementary steps of Ni( ii )-catalyzed C(sp 2 )–H iodination with I 2 and substrates bearing N , N ′-bidentate directing centers, amide-oxazoline (AO) and 8-aminoquinoline (AQ). The relative stability of the lowest energy high- and low-spin electronic states of the catalyst and intermediates is found to be an important factor for all of the steps in the reaction. As a result, two-state reactivity for these systems is reported, where the reaction is initiated on the triplet surface and generates a high energy singlet nickelacycle. It is shown that the addition of Na 2 CO 3 base to the reaction mixture facilitates C–H activation. The presence of I 2 in the reaction provides the much needed driving force for the C–H activation and nickelacycle formation and ultimately reacts to form a new C–I bond through either a redox neutral electrophilic cleavage (EC) pathway or a one-electron reductive cleavage (REC) pathway. The previously proposed Ni( ii )/Ni( iv ) and homolytic cleavage pathways are found to be higher in energy. The nature of the substrate is found to have a large impact on the relative stability of the lowest electronic states and on the stability of the nickelacycle resulting from C–H activation. 

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5. A cyanide-bridged wheel featuring a seven-coordinate Mo( iii ) center

   https://doi.org/10.1039/c8cc09373c  

   Kempe, David K.; Dolinar, Brian S.; Vignesh, Kuduva R.; Woods, Toby J.; Saber, Mohamed R.; Dunbar, Kim R. (February 2019, Chemical Communications)

   A new cyclic molecule incorporating [Mo III (CN) 7 ] 4− has been characterized by single crystal X-ray methods, SQUID magnetometry and theoretical calculations. The wheel molecule [Mo III (CN) 7 ] 6 [Ni(L)] 12 (H 2 O) 6 exhibits ferromagnetic Mo–Ni coupling which did not exist for the previously reported octacyanometallate analogue [Mo IV (CN) 8 ] 6 [Ni(L)] 12 (H 2 O) 6 . These results indicate that known supramolecular architectures incorporating octacyanometallates can be used as platforms for making new molecules incorporating seven-coordinate cyanide precursors. 

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