Unsymmetrical coordinated Ag(I)–olefin complex based on exo-7-oxabicyclo-[2.2.1]-5-heptene-2,3-dicarboxylate: Synthesis, structure and electrocatalytical property

Hartley, 1973, Thermodynamic data for olefin and acetylene complexes of transition metals, Chem. Rev., 73, 163, 10.1021/cr60282a005 Ho, 1988, Olefin separations via complexation with cuprous diketonate, Ind. Eng. Chem. Res., 27, 334, 10.1021/ie00074a021 Reisinger, 2009, Silver–ethene complexes [Ag(η2-C2H4)n][Al(ORF)4] with n=1, 2, 3 (RF=fluorine-substituted group), Chem. Eur. J., 15, 9505, 10.1002/chem.200900100 Huang, 1999, Anion and cation effects on olefin adsorption on silver and copper halides: ab initio effective core potential study of π-complexation, J. Phys. Chem. B, 103, 3206, 10.1021/jp982857c Hong, 2000, Polymer–salt complexes containing silver ions and their application to facilitated olefin transport membranes, Adv. Mater., 12, 968, 10.1002/1521-4095(200006)12:13<968::AID-ADMA968>3.0.CO;2-W Ryu, 2001, Facilitated olefin transport by reversible olefin coordination to silver ions in a dry cellulose acetate membrane, Chem. Eur. J., 7, 1525, 10.1002/1521-3765(20010401)7:7<1525::AID-CHEM1525>3.0.CO;2-U Crabtree, 2001 Defieber, 2008, Chiral olefins as steering ligands in asymmetric catalysis, Angew. Chem. Int. Ed., 47, 4482, 10.1002/anie.200703612 Maire, 2004, Olefins as steering ligands for homogeneously catalyzed hydrogenations, Chem. Eur. J., 10, 4198, 10.1002/chem.200400441 Johnson, 2008, More than bystanders: the effect of olefins on transition-metal-catalyzed cross-coupling reactions, Angew. Chem. Int. Ed., 47, 840, 10.1002/anie.200700278 Bruin, 2004, Functional models for rhodium-mediated olefin-oxygenation catalysis, Angew. Chem. Int. Ed., 43, 4142, 10.1002/anie.200300629 Cedeńo, 2001, Experimental determination of the Cr–C2Cl4 bond dissociation enthalpy in Cr(CO)5(C2Cl4): quantifying metal−olefin bonding interactions, J. Am. Chem. Soc., 123, 12857, 10.1021/ja011643x Carpentier, 2001, Solution structures and dynamic properties of chelated d0 metal olefin complexes {η5: η1-C5R4SiMe2NtBu}Ti(OCMe2CH2CH2CH═CH2)+ (R=H, Me): Models for the {η5: η1-C5R4SiMe2NtBu}Ti(R′)(olefin)+ intermediates in “constrained geometry” catalysts, J. Am. Chem. Soc., 123, 898, 10.1021/ja003209l Choualeb, 2007, Olefin complexes of low-valent rhenium, Eur. J. Inorg. Chem., 5246, 10.1002/ejic.200700573 Chahboun, 2009, Insight into cis-to-trans olefin isomerisation catalysed by group 4 and 6 cyclopentadienyl compounds, Eur. J. Inorg. Chem., 1514, 10.1002/ejic.200900069 Cedeno, 2005, Metal–olefin interactions in M(CO)5(cycloolefin) (M=Cr, Mo, W; cycloolefin=cyclopropene to cyclooctene): strain relief and metal−olefin bond strength, Organometallics, 24, 3882, 10.1021/om050331q Schlappi, 2003, Electron-withdrawing effects on metal−olefin bond strengths in Ni(PH3)2(CO)(C2XnH4−n), X=F, Cl; n=0–4: a DFT Study, J. Phys. Chem. A, 107, 8763, 10.1021/jp0357572 Mccluskeya, 2000, Anhydride modified cantharidin analogues. Is ring opening important in the inhibition of protein phosphatase 2A?, Eur. J. Med. Chem., 35, 957, 10.1016/S0223-5234(00)00186-0 Stockmann, 1961, On the titrimetric determination of the configuration of bridged Diels–Alder adducts, J. Org. Chem., 26, 2025, 10.1021/jo01065a084 Gong, 2012, CrystEngComm, 14, 663, 10.1039/C1CE05846K Turner, 2004, Sustainable Hydrogen Production, Science, 305, 972, 10.1126/science.1103197 Sun, 2011, Molecular cobalt pentapyridine catalysts for generating hydrogen from water, J. Am. Chem. Soc., 133, 9212, 10.1021/ja202743r Jain, 2011, Incorporating peptides in the outer-coordination sphere of bioinspired electrocatalysts for hydrogen production, Inorg. Chem., 50, 4073, 10.1021/ic1025872 Voloshin, 2011, Efficient electrocatalytic hydrogen production from H+ ions using specially designed boron-capped cobalt clathrochelates, Chem. Commun., 47, 7737, 10.1039/c1cc12239h Blatov, 2006, IUCr CompComm, Newsletter, 7, 4 Zhou, 2007, Template-synthesized cobalt porphyrin/polypyrrole nanocomposite and its electrocatalysis for oxygen reduction in neutral medium, J. Phys. Chem. C, 111, 11216, 10.1021/jp072390i Yu, 2005, Molecular films of water-miscible ionic liquids formed on glassy carbon electrodes: characterization and electrochemical applications, Langmuir, 21, 9000, 10.1021/la051089v Su, 2010, Molecular electrocatalysis for oxygen reduction by cobalt porphyrins adsorbed at liquid/liquid interfaces, J. Am. Chem. Soc., 132, 2655, 10.1021/ja908488s Chen, 2007, An effective hydrothermal route for the synthesis of multiple PDDA-protected noble-metal nanostructures, Inorg. Chem., 46, 10587, 10.1021/ic7009572 Cheng, 1996, Electrochemical behavior of the molybdotungstate heteropoly complex with neodymium, K10H3[Nd(SiMo7W4O39)2] · xH2O in aqueous solution, J. Electroanal. Chem., 407, 97, 10.1016/0022-0728(95)04466-3 Wang, 2006, Self-assembly of nanometer-scale [Cu24I10L12]14+ cages and ball-shaped Keggin clusters into a (4,12)-connected 3D framework with photoluminescent and electrochemical properties, Angew. Chem. Int. Ed., 45, 7411, 10.1002/anie.200603250 Zhang, 2011, The factors affecting on the assembly of Ag–H2biim system: size, charge or shape of polyanions?, CrystEngComm, 13, 3832, 10.1039/c1ce05093a Yang, 2010, A metal–organic framework as an electrocatalyst for ethanol oxidation, Angew. Chem. Int. Ed., 49, 5348, 10.1002/anie.201000863 Wang, 2010, Self-assembly of nanometre-scale metallacalix[4]arene building blocks and Keggin units to a novel (3,4)-connected 3D self-penetrating framework, Chem. Commun., 46, 6485, 10.1039/c0cc01412e Liu, 2010, Engineering homochiral metal–organic frameworks for heterogeneous asymmetric catalysis and enantioselective separation, Adv. Mater., 22, 4112, 10.1002/adma.201000197 Yi, 2011, Metal–organic frameworks with achiral/monochiral nano-channels, Cryst. Growth Des., 11, 2824, 10.1021/cg101618n Ma, 2009, Enantioselective catalysis with homochiral metal–organic frameworks, Chem. Soc. Rev., 38, 1248, 10.1039/b807083k Sun, 2006, Spontaneous resolution of silver double helicates consisting of achiral ligands with several aromatic rings, Chem. Commun., 26, 2777, 10.1039/b604066g