Spectroelectrochemical evidence for communication within a laterally-bridged dimanganese(III) bis-porphyrin.

نویسندگان

  • Robert S Armstrong
  • Garry J Foran
  • Warren A Hough
  • Deanna M D'Alessandro
  • Peter A Lay
  • Maxwell J Crossley
چکیده

Electronic coupling between the porphyrin units of a laterally-bridged dimanganese(III) bis-porphyrin 2 is explored using electrochemistry, spectroelectrochemistry and resonance-Raman spectroscopy. It is found that strong electronic interactions between the manganese(III) ion and the porphyrin macrocycle enhance the perturbations experienced by these bis-porphyrin systems when compared to related monomer porphyrin systems. In turn this leads to effective electronic communication between the manganese ions in the bis-porphyrin. This finding has importance in the design of molecular wires based on laterally-bridged oligo-metallo-porphyrins.

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

Synthesis and characterization of xanthene-bridged Schiff-base dimanganese(III) complexes: bimetallic catalysts for asymmetric oxidation of sulfides.

Dimanganese(III) complexes of salen-type ligands anchored by 9,9-dimethylxanthene-4,5-diyl spacers were synthesized. Two types of structures, cyclic and acyclic forms, are presented. The 2 + 2 Schiff-base condensation of 5,5'-(9,9-dimethylxanthene-4,5-diyl)bis(salicylaldehyde) and 1,2-diaminobenzene gave a macrocyclic ligand, from which a cyclic dimanganese(III) complex was synthesized. A simil...

متن کامل

Titanium and manganese complexes supported by a xanthene-bridged bis(tripodal N2O2) ligand: isomerization, intramolecular hydrogen bonding and metal-binding ability.

A new bis(N2O2) ligand, L(4-), in which two tripodal diamine-bis(phenolate) moieties are bridged by a xanthene backbone, was prepared. The reaction of H4L with 2 equiv. of [Ti(O(i)Pr)4] produced C2 and Cs symmetrical isomers of the dititanium(IV,IV) complex [Ti2(L)(O(i)Pr)4]. The isolated C2 isomer was slowly converted to the Cs isomer via Ti-N bond cleavage to form a 3 : 2 mixture in equilibri...

متن کامل

Reaction landscape of a pentadentate N5-ligated Mn(II) complex with O2˙- and H2O2 includes conversion of a peroxomanganese(III) adduct to a bis(μ-oxo)dimanganese(III,IV) species.

Herein we describe the chemical reactivity of the mononuclear [Mn(II)(N4py)(OTf)](OTf) (1) complex with hydrogen peroxide and superoxide. Treatment of 1 with one equivalent superoxide at -40 °C in MeCN formed the peroxomanganese(III) adduct, [Mn(III)(O2)(N4py)](+) (2) in ~30% yield. Complex 2 decayed over time and the formation of the bis(μ-oxo)dimanganese(III,IV) complex, [Mn(III)Mn(IV)(μ-O)2(...

متن کامل

Excitonic coupling interactions in the self-assembly of perylene-bridged bis(β-cyclodextrin)s and porphyrin.

A supramolecular self-assembly has been constructed by perylene-bridged bis(β-cyclodextrin)s with water-soluble porphyrin through hydrophobic interactions, showing strong excitonic coupling interactions between perylene backbones and included porphyrins.

متن کامل

A combined computational and spectroelectrochemical study of platinum-bridged bis-triarylamine systems.

The character of the electronic transitions in the ultraviolet-visible-near infrared (UV-vis-NIR) spectra of platinum-bis(alkynyl) bridged, bis-triarylamine mixed-valence systems trans-[Pt(C≡CC6H4NAr2)2 (PR3)2](n+) (R = ethyl, Ar = C6H4CH3-4 (1) or C6H4OCH3-4 (2); R = Ph, Ar = C6H4CH3-4 (3) or C6H4OCH3-4 (4), n = 0, 1, 2) has been determined from a combination of spectroscopic measurement and d...

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:
  • Dalton transactions

دوره 40  شماره 

صفحات  -

تاریخ انتشار 2006