Cofacial dicobalt complex of a binucleating hexacarboxamide cryptand ligand.

نویسندگان

  • Glen E Alliger
  • Peter Müller
  • Christopher C Cummins
  • Daniel G Nocera
چکیده

A hexacarboxamide cryptand featuring appended polyether moieties is used as a binucleating ligand for two Co(II) centers, marking the first time cryptands have been used as hexaanionic N donors for metal coordination. A synthesis for the hexacarboxamide cryptand, culminating in a 23% yield high-dilution step and proceeding in 8% overall yield, is reported. The ligand is metalated using cobalt(II) acetate, and a solid-state structure is presented, revealing an intermetallic void over 6.4 A in length. The reactivity of this new type of cryptate is also probed; treatment of the dicobalt cryptate with potassium cyanide at elevated temperature results in a bridging cyanide complex.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Multi-electron reactivity of a cofacial di-tin(ii) cryptand: partial reduction of sulfur and selenium and reversible generation of S3˙.

Cofacial bimetallic tin(ii) ([Sn2(mBDCA-5t)]2-, 1) and lead(ii) ([Pb2(mBDCA-5t)]2-, 2) complexes have been prepared by hexadeprotonation of hexacarboxamide cryptand mBDCA-5t-H6 together with double Sn(ii) or Pb(ii) insertion. Reaction of 1 with elemental sulfur or selenium generates di-tin polychalcogenide complexes containing μ-E and bridging μ-E5 ligands where E = S or Se, and the Sn(ii) cent...

متن کامل

Family of cofacial bimetallic complexes of a hexaanionic carboxamide cryptand.

A series of coordination compounds has been prepared comprising manganese, iron, nickel, and zinc bound by a hexaanionic cryptand where carboxamides are anionic N-donors. The metal complexes have been investigated by X-ray crystallography, and possess metal centers in trigonal monopyramidal geometries with intermetallic distances spanning d(Mn,avg) = 6.080 Å to d(Ni,avg) = 6.495 Å. All complexe...

متن کامل

Ligand modifications for tailoring the binuclear microenvironments in Schiff-base calixpyrrole pacman complexes.

The synthesis and structures of two new octadentate, Schiff-base calixpyrrole macrocycles are presented in which modifications at the meso-substituents (L(1)) or the aryl spacer between the two pyrrole-imine donor compartments (L(2)) are introduced. The outcomes of these changes are highlighted in the structures of binuclear Pacman complexes of these macrocycles, [M(2)(L(1))] and [M(2)(L(2))]. ...

متن کامل

Nickel complexes of a binucleating ligand derived from an SCS pincer.

A binucleating ligand has been prepared that contains an SCS pincer and three oxygen donor atoms in a partial crown ether loop. To enable metalation with Ni(0), a bromoarene precursor was used and resulted in the formation of a nickel-bromide complex in the SCS pincer portion of the ligand. Reaction of the nickel complex with a lithium salt yielded a heterobimetallic complex with bromide bridgi...

متن کامل

Electron-transfer studies of a peroxide dianion.

A peroxide dianion (O2(2-)) can be isolated within the cavity of hexacarboxamide cryptand, [(O2)⊂mBDCA-5t-H6](2-), stabilized by hydrogen bonding but otherwise free of proton or metal-ion association. This feature has allowed the electron-transfer (ET) kinetics of isolated peroxide to be examined chemically and electrochemically. The ET of [(O2)⊂mBDCA-5t-H6](2-) with a series of seven quinones,...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Inorganic chemistry

دوره 49 8  شماره 

صفحات  -

تاریخ انتشار 2010