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Title: The synthesis of PNP-supported low-spin nitro manganese(I) carbonyl complexes

In this study, the coordination chemistry of Mn(CO)5Br was investigated with a series of PNP-pincer ligands. The ligands iPrPONOP (iPrPONOP = 2,6-bis(diisopropylphosphinito)pyridine) and iPrPNHP (iPrPNHP = HN{CH2CH2(PiPr2)}2) gave the desired organometallic manganese complexes (iPrPONOP)Mn(CO)2Br and (iPrPNHP)Mn(CO)2Br, respectively, upon chelation to Mn(CO)5Br. The reactivity of iPrPNNNP (iPrPNNNP = N,N'-bis(diisopropylphosphino)-2,6-diaminopyridine) with Mn(CO)5Br yielded a pair of products, [(iPrPNNNP)Mn(CO)3][Br] and (iPrPNNNCO)Mn(CO)3. The formation of the asymmetric chelate arises from a formal loss of iPr2PBr and C–N bond formation from a carbonyl ligand and NH, yielding a Mn(I) amide core. The nitration reactions of (iPrPONOP)Mn(CO)2Br and (iPrPNHP)Mn(CO)2Br were carried out using silver nitrite, yielding the nitro compounds (iPrPONOP)Mn(CO)2(NO2) and (iPrPNHP)Mn(CO)2(NO2), respectively. The analogous iron complex (iPrPONOP)Fe(CO)Cl2 was nitrated under the same conditions to yield the salt pair [(iPrPONOP)Fe(CO)2][FeCl3NO]. This reactivity underlines the difference between iso-valent iron and manganese centers. The manganese complexes (iPrPONOP)Mn(CO)2(NO2) and (iPrPNHP)Mn(CO)2(NO2) were ineffective as oxygen atom transfer reagents for a variety of substrates.
 [1] ;  [1]
  1. Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
Publication Date:
OSTI Identifier:
Report Number(s):
Journal ID: ISSN 0277-5387; PII: S0277538716300791
Grant/Contract Number:
Accepted Manuscript
Journal Name:
Additional Journal Information:
Journal Name: Polyhedron; Journal ID: ISSN 0277-5387
Research Org:
Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
Sponsoring Org:
Country of Publication:
United States
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY manganese; multidentate ligands; synthesis; nitro compounds; nitrosyl ligands