ABSTRACT
Oligo- and polyazulenes are attractive π-conjugated building blocks in designing advanced functional materials. Herein, we demonstrate that anchoring one or both isocyanide termini of the redox non-innocent 2,2'-diisocyano-6,6'-biazulenic π-linker (1) to the redox-active [Cr(CO)5] moiety provided a convenient intramolecular redox reference for unambiguously establishing that the 6,6'-biazulenic scaffold undergoes a reversible one-step 2e- reduction governed by reduction potential compression/inversion. Treatment of bis(η6-naphthalene)chromium(0) with six equiv. of 2-isocyano-1,1',3,3'-tetraethoxycarbonyl-6,6'-biazulene (6) or [(OC)5Cr(η1-2,2'-diisocyano-1,1',3,3'-tetraethoxycarbonyl-6,6'-biazulene)] (11) afforded homoleptic Cr(0) complexes 13 and 14 with a 12e- (per molecule) ligand-based reduction capacity at mild E1/2 of -1.29 V and -1.15 V vs. Cp2Fe0/+, respectively. The overall reversible redox capacity varies from 15e- for the mononuclear complex 13 to 21e- for the heptanuclear complex 14. The latter "nanocomplex" has a diameter of ca. 5 nm and features seven Cr(0) centers interlinked with six 2,2'-diisocyano-6,6'-biazulenic bridges. The X-ray structure of [(OC)5Cr(2-isocyano-1,1',3,3'-tetraethoxycarbonyl-6,6'-biazulene)] (7) indicated a 43.5° interplanar angle between the two azulenic moieties. Self-assembly of 11 on a Au(111) substrate afforded an organometallic monolayer film of 11 featuring approximately upright orientation of the 2,2'-diisocyano-6,6'-biazulenic linkers, as evidenced by ellipsometric measurements and the RAIR signature of the C4v-symmetric [(-NC)Cr(CO)5] infrared reporter within 11. Remarkably, comparing the FTIR spectrum of 11 in solution with the RAIR spectrum of 11 adsorbed on Au(111) suggested electronic coupling at a ca. 2 nm distance between the Cr(0) and Au atoms linked by the 2,2'-diisocyano-6,6'-biazulene bridge.
ABSTRACT
Mercapto (-SH) and isocyano (-N≡C) terminated conducting π-linkers are often employed in the ever-growing quest for organoelectronic materials. While such systems typically involve symmetric dimercapto or diisocyano anchoring of the organic bridge, this article introduces the chemistry of a linear azulenic π-linker equipped with one mercapto and one isocyano terminus. The 2-isocyano-6-mercaptoazulene platform was efficiently accessed from 2-amino-6-bromo-1,3-diethoxycarbonylazulene in four steps. The 2-N≡C end of this 2,6-azulenic motif was anchrored to the [Cr(CO)5] fragment prior to formation of its 6-SH terminus. Metalation of the 6-SH end of [(OC)5Cr(η1-2-isocyano-1,3-diethoxycarbonyl-6-mercaptoazulene)] (7) with Ph3PAuCl, under basic conditions, afforded X-ray structurally characterized heterobimetallic Cr0/AuI ensemble [(OC)5Cr(µ-η1:η1-2-isocyano-1,3-diethoxycarbonyl-6-azulenylthiolate)AuPPh3] (8). Analysis of the 13C NMR chemical shifts for the [(NC)Cr(CO)5] core in a series of the related complexes [(OC)5Cr(2-isocyano-6-X-1,3-diethoxy-carbonylazulene)] (X = -N≡C, Br,H, SH, SCH2CH2CO2CH2CH3, SAuPPh3) unveiled remarkably consistent inverse-linear correlations δ( 13COtrans) vs. δ( 13CN) and δ( 13COcis) vs. δ( 13CN) that appear to hold well beyond the above 2-isocyanoazulenic series to include complexes [(OC)5Cr(CNR)] containing strongly electron-withdrawing substituents R, such as CF3, CFClCF2Cl, C2F3, and C6F5. In addition to functioning as asensitive 13C NMR handle, the essentially C4v-symmetric [(-NC)Cr(CO)5] moiety proved to be an informative, remote, νN≡C/νC≡O infrared reporter in probing chemisorption of 7 on the Au(111) surface.
