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Cages on Surfaces: Thiol Functionalisation of Co III Sarcophagine Complexes
Author(s) -
Harrowfield Jack M.,
Koutsantonis George A.,
Kraatz HeinzBernhard,
Nealon Gareth L.,
Orlowski Grzegorz A.,
Skelton Brian W.,
White Allan H.
Publication year - 2007
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200600626
Subject(s) - chemistry , crystal structure , deprotonation , crystallography , cobalt , stereochemistry , inorganic chemistry , ion , organic chemistry
A number of new (sarcophagine)cobalt compounds containing oligopeptide substituents terminated by a mercaptoethylamide unit, [Co(R)(R′)sar] 2 6+ (R = NH 2 , CH 3 ; R′ = NHpeptideCONHCH 2 CH 2 S–), have been prepared utilising the carboxymethyl complexes [Co(R){N(CH 2 CO 2 H)}sar] 3+ (R = NH 2 , CH 3 ), and subsequently characterised. The amino acid residues, terminating with cystamine groups, were introduced into the carboxymethyl complexes using standard peptide coupling chemistry. The solid‐state structures of [Co(CH 3 ){N(CH 2 CO 2 H)}sar]Cl 4 · H 2 O, [Co(CH 3 ){N(CH 2 CO 2 H) 2 }sar]Cl 3 · 2H 2 O and [Co(CH 3 ){N(CH 2 CO 2 ) 2 }sar]Cl · 6.5H 2 O were determined by single‐crystal X‐ray diffraction experiments, the first two forming lattices containing homochiral sheets of cations in planes parallel to [0,0,1]. In the structure of [Co(CH 3 ){N(CH 2 CO 2 H)}sar]Cl 4 · H 2 O, the cations are of the same absolute configuration, but this alternates from one sheet tothe next. In the dihydrate, [Co(CH 3 ){N(CH 2 CO 2 H) 2 }sar]Cl 3 · 2H 2 O, the structure appears to be very similar. The sheet alternation is different from the structure of the monohydrate, [Co(CH 3 ){N(CH 2 CO 2 H)}sar]Cl 4 · H 2 O. The deprotonated imidodiacetate complex, [Co(CH 3 ){N(CH 2 CO 2 ) 2 }sar]Cl · 6.5H 2 O, was prepared in an unrelated reaction; the structure displays hydogen‐bonding interactions involving the carboxylate groups and coordinated NH units. The solution electrochemistry of these compounds has been investigated using both cyclic voltammetry and differential pulse voltammetry. The compounds exhibited pH‐dependent, quasi‐reversible redox behaviour. A monolayer was prepared by the interaction of [Co(R)sar(GlyNHCH 2 CH 2 S–)] 2 6+ and a gold microelectrode using both conventional “self assembly” (SAM) and electrodeposition (EDM) techniques. Surface cyclic voltammograms were measured, which, after a period of induction associated with surface reorganisation, were typical of an ordered monolayer. The monolayer was characterised by XPS, showing peaks assigned to the presence of S, Co, N, O and C. Ellipsometry gave a film thickness of 7 ± 1 Å, consistent with the formation of a mono‐ rather than a multi‐layer. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)