Gold(I) and Silver(I) π-Complexes with Unsaturated Hydrocarbons
Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
34054181
PubMed Central
PMC8155574
DOI
10.1021/acs.organomet.1c00143
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
Gold π-complexes have been studied largely in the past 2 decades because of their role in gold-catalyzed reactions. We report an experimental and theoretical investigation of the interaction between a wide range of unsaturated hydrocarbons (alkanes, alkynes, alkadienes, and allenes) and triphenylphosphine-gold(I), triphenylphosphine-silver(I), and acetonitrile-silver(I) cations. The bond dissociation energies of these complexes were determined by mass spectrometry collision-induced dissociations and their structures were studied by density functional theory calculations and infrared photodissociation spectroscopy. The results show that with the same phosphine ligand, gold binds stronger to the π-ligands than silver and thereby activates the unsaturated bond more effectively. Ligand exchange of phosphine by acetonitrile at the silver complexes increases the binding energy as well as the activation of the π-ligands. We also show that the substitution of an unsaturated bond is more important than the bond type.
Zobrazit více v PubMed
Hashmi A. S. K.; Hutchings G. J. Gold Catalysis. Angew. Chem., Int. Ed. 2006, 45, 7896–7936. 10.1002/anie.200602454. PubMed DOI
Gorin D. J.; Toste F. D. Relativistic effects in homogeneous gold catalysis. Nature 2007, 446, 395–403. 10.1038/nature05592. PubMed DOI
Hashmi A. S. K. Gold-Catalyzed Organic Reactions. Chem. Rev. 2007, 107, 3180–3211. 10.1021/cr000436x. PubMed DOI
Hashmi A. S. K.; Rudolph M. Gold catalysis in total synthesis. Chem. Soc. Rev. 2008, 37, 1766–1775. 10.1039/b615629k. PubMed DOI
Rudolph M.; Hashmi A. S. K. Gold catalysis in total synthesis-an update. Chem. Soc. Rev. 2012, 41, 2448–2462. 10.1039/c1cs15279c. PubMed DOI
Friend C. M.; Hashmi A. S. K. Gold Catalysis. Acc. Chem. Res. 2014, 47, 729–730. 10.1021/ar5000506. PubMed DOI
Hashmi A. S. K. Dual Gold Catalysis. Acc. Chem. Res. 2014, 47, 864–876. 10.1021/ar500015k. PubMed DOI
Zhang L. A Non-Diazo Approach to α-Oxo Gold Carbenes via Gold-Catalyzed Alkyne Oxidation. Acc. Chem. Res. 2014, 47, 877–888. 10.1021/ar400181x. PubMed DOI PMC
Wang Y.-M.; Lackner A. D.; Toste F. D. Development of Catalysts and Ligands for Enantioselective Gold Catalysis. Acc. Chem. Res. 2014, 47, 889–901. 10.1021/ar400188g. PubMed DOI PMC
Obradors C.; Echavarren A. M. Gold-Catalyzed Rearrangements and Beyond. Acc. Chem. Res. 2014, 47, 902–912. 10.1021/ar400174p. PubMed DOI PMC
Zhang D.-H.; Tang X.-Y.; Shi M. Gold-Catalyzed Tandem Reactions of Methylenecyclopropanes and Vinylidenecyclopropanes. Acc. Chem. Res. 2014, 47, 913–924. 10.1021/ar400159r. PubMed DOI
Fürstner A. From Understanding to Prediction: Gold- and Platinum-Based π-Acid Catalysis for Target Oriented Synthesis. Acc. Chem. Res. 2014, 47, 925–938. 10.1021/ar4001789. PubMed DOI
Alcaide B.; Almendros P. Gold-Catalyzed Cyclization Reactions of Allenol and Alkynol Derivatives. Acc. Chem. Res. 2014, 47, 939–952. 10.1021/ar4002558. PubMed DOI
Fensterbank L.; Malacria M. Molecular Complexity from Polyunsaturated Substrates: The Gold Catalysis Approach. Acc. Chem. Res. 2014, 47, 953–965. 10.1021/ar4002334. PubMed DOI
Yeom H.-S.; Shin S. Catalytic Access to α-Oxo Gold Carbenes by N–O Bond Oxidants. Acc. Chem. Res. 2014, 47, 966–977. 10.1021/ar4001839. PubMed DOI
Hashmi A. S. K. Homogeneous Gold Catalysis Beyond Assumptions and Proposals—Characterized Intermediates. Angew. Chem., Int. Ed. 2010, 49, 5232–5241. 10.1002/anie.200907078. PubMed DOI
Pernpointner M.; Hashmi A. S. K. Fully Relativistic, Comparative Investigation of Gold and Platinum Alkyne Complexes of Relevance for the Catalysis of Nucleophilic Additions to Alkynes. J. Chem. Theory Comput. 2009, 5, 2717–2725. 10.1021/ct900441f. PubMed DOI
Brooner R. E. M.; Widenhoefer R. A. Cationic, Two-Coordinate Gold π Complexes. Angew. Chem., Int. Ed. 2013, 52, 11714–11724. 10.1002/anie.201303468. PubMed DOI
Lauterbach T.; Asiri A. M.; Hashmi A. S. K. Organometallic Intermediates of Gold Catalysis. Adv. Organomet. Chem. 2014, 62, 261–297. 10.1016/b978-0-12-800976-5.00005-9. DOI
Jones A. C.Gold π-Complexes as Model Intermediates in Gold Catalysis. In Homogeneous Gold Catalysis; Slaughter L. M., Ed.; Springer International Publishing: Cham, 2015, pp 133–165. PubMed
Jašíková L.; Anania M.; Hybelbauerová S.; Roithová J. Reaction Intermediates Kinetics in Solution Investigated by Electrospray Ionization Mass Spectrometry: Diaurated Complexes. J. Am. Chem. Soc. 2015, 137, 13647–13657. 10.1021/jacs.5b08744. PubMed DOI
Wang D.; Cai R.; Sharma S.; Jirak J.; Thummanapelli S. K.; Akhmedov N. G.; Zhang H.; Liu X.; Petersen J. L.; Shi X. “Silver Effect” in Gold(I) Catalysis: An Overlooked Important Factor. J. Am. Chem. Soc. 2012, 134, 9012–9019. 10.1021/ja303862z. PubMed DOI
Homs A.; Escofet I.; Echavarren A. M. On the Silver Effect and the Formation of Chloride-Bridged Digold Complexes. Org. Lett. 2013, 15, 5782–5785. 10.1021/ol402825v. PubMed DOI PMC
Zhu Y.; Day C. S.; Zhang L.; Hauser K. J.; Jones A. C. A Unique Au–Ag–Au Triangular Motif in a Trimetallic Halonium Dication: Silver Incorporation in a Gold(I) Catalyst. Chem.—Eur. J. 2013, 19, 12264–12271. 10.1002/chem.201302152. PubMed DOI
Lu Z.; Han J.; Hammond G. B.; Xu B. Revisiting the Influence of Silver in Cationic Gold Catalysis: A Practical Guide. Org. Lett. 2015, 17, 4534–4537. 10.1021/acs.orglett.5b02224. PubMed DOI
Zhdanko A.; Maier M. E. Explanation of “Silver Effects” in Gold(I)-Catalyzed Hydroalkoxylation of Alkynes. ACS Catal. 2015, 5, 5994–6004. 10.1021/acscatal.5b01493. DOI
Jia M.; Bandini M. Counterion Effects in Homogeneous Gold Catalysis. ACS Catal. 2015, 5, 1638–1652. 10.1021/cs501902v. DOI
Yang Y.; Antoni P.; Zimmer M.; Sekine K.; Mulks F. F.; Hu L.; Zhang L.; Rudolph M.; Rominger F.; Hashmi A. S. K. Dual Gold/Silver Catalysis Involving Alkynylgold(III) Intermediates Formed by Oxidative Addition and Silver-Catalyzed C–H Activation for the Direct Alkynylation of Cyclopropenes. Angew. Chem., Int. Ed. 2019, 58, 5129–5133. 10.1002/anie.201812577. PubMed DOI
Hu L.; Dietl M. C.; Han C.; Rudolph M.; Rominger F.; Hashmi A. S. K. Au-Ag Bimetallic Catalysis Providing 3-Alkynyl Benzofurans from Phenols via Tandem C-H Alkynylation/Oxy-Alkynylation. Angew. Chem., Int. Ed. 2021, 60, 106337–10642. 10.1002/anie.202016595. PubMed DOI PMC
Škríba A.; Jašíková L.; Roithová J. Silver(I) and gold(I) complexes of diethylmalonate. Int. J. Mass Spectrom. 2012, 330–332, 226–232. 10.1016/j.ijms.2012.08.019. DOI
Jašíková L.; Roithová J. Interaction of Gold Acetylides with Gold(I) or Silver(I) Cations. Organometallics 2013, 32, 7025–7033. 10.1021/om4006774. DOI
Schröder D. Applications of Electrospray Ionization Mass Spectrometry in Mechanistic Studies and Catalysis Research. Acc. Chem. Res. 2012, 45, 1521–1532. 10.1021/ar3000426. PubMed DOI
Roithová J.; Janková Š.; Jašíková L.; Váňa J.; Hybelbauerová S. Gold–Gold Cooperation in the Addition of Methanol to Alkynes. Angew. Chem., Int. Ed. 2012, 51, 8378–8382. 10.1002/anie.201204003. PubMed DOI
Jašíková L.; Roithová J. Interaction of the Gold(I) Cation Au(PMe3)+ with Unsaturated Hydrocarbons. Organometallics 2012, 31, 1935–1942. 10.1021/om2012387. DOI
Schulz J.; Jašíková L.; Škríba A.; Roithová J. Role of Gold(I) α-Oxo Carbenes in the Oxidation Reactions of Alkynes Catalyzed by Gold(I) Complexes. J. Am. Chem. Soc. 2014, 136, 11513–11523. 10.1021/ja505945d. PubMed DOI
Dorel R.; Echavarren A. M. Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity. Chem. Rev. 2015, 115, 9028–9072. 10.1021/cr500691k. PubMed DOI PMC
Zuccaccia D.; Belpassi L.; Tarantelli F.; Macchioni A. Ion Pairing in Cationic Olefin–Gold(I) Complexes. J. Am. Chem. Soc. 2009, 131, 3170–3171. 10.1021/ja809998y. PubMed DOI
Brooner R. E. M.; Brown T. J.; Widenhoefer R. A. Synthesis and Study of Cationic, Two-Coordinate Triphenylphosphine– Gold−π Complexes. Chem.—Eur. J. 2013, 19, 8276–8284. 10.1002/chem.201204564. PubMed DOI
Motloch P.; Blahut J.; Císařová I.; Roithová J. X-ray characterization of triphenylphosphine-gold(I) olefin π-complexes and the revision of their stability in solution. J. Organomet. Chem. 2017, 848, 114–117. 10.1016/j.jorganchem.2017.07.011. DOI
Shapiro N. D.; Toste F. D. Synthesis and structural characterization of isolable phosphine coinage metal π-complexes. Proc. Natl. Acad. Sci. U.S.A. 2008, 105, 2779–2782. 10.1073/pnas.0710500105. DOI
Hooper T. N.; Green M.; McGrady J. E.; Patel J. R.; Russell C. A. Synthesis and structural characterisation of stable cationic gold(i) alkene complexes. Chem. Commun. 2009, 3877–3879. 10.1039/b908109g. PubMed DOI
Zhu Y.; Day C. S.; Jones A. C. Synthesis and Structure of Cationic Phosphine Gold(I) Enol Ether Complexes. Organometallics 2012, 31, 7332–7335. 10.1021/om300893q. DOI
Grirrane A.; Álvarez E.; Albero J.; García H.; Corma A. Multinuclear silver(i) XPhos complexes with cyclooctatetraene: photochemical C–C bond cleavage of acetonitrile and cyanide bridged Ag cluster formation. Dalton Trans. 2016, 45, 5444–5450. 10.1039/c6dt00370b. PubMed DOI
Griebel C.; Hodges D. D.; Yager B. R.; Liu F. L.; Zhou W.; Makaravage K. J.; Zhu Y.; Norman S. G.; Lan R.; Day C. S.; Jones A. C. Bisbiphenyl Phosphines: Structure and Synthesis of Gold(I) Alkene π-Complexes with Variable Phosphine Donicity and Enhanced Stability. Organometallics 2020, 39, 2665–2671. 10.1021/acs.organomet.0c00278. DOI
Ridlen S. G.; Wu J.; Kulkarni N. V.; Dias H. V. R. Isolable Ethylene Complexes of Copper(I), Silver(I), and Gold(I) Supported by Fluorinated Scorpionates [HB{3-(CF3),5-(CH3)Pz}3]– and [HB{3-(CF3),5-(Ph)Pz}3]–. Eur. J. Inorg. Chem. 2016, 2016, 2573–2580. 10.1002/ejic.201501365. DOI
Klimovica K.; Kirschbaum K.; Daugulis O. Synthesis and Properties of “Sandwich” Diimine-Coinage Metal Ethylene Complexes. Organometallics 2016, 35, 2938–2943. 10.1021/acs.organomet.6b00487. PubMed DOI PMC
Navarro M.; Toledo A.; Joost M.; Amgoune A.; Mallet-Ladeira S.; Bourissou D. π Complexes of P̂P and P̂N chelated gold(i). Chem. Commun. 2019, 55, 7974–7977. 10.1039/c9cc04266k. PubMed DOI
Navarro M.; Toledo A.; Mallet-Ladeira S.; Sosa Carrizo E. D.; Miqueu K.; Bourissou D. Versatility and adaptative behaviour of the P̂N chelating ligand MeDalphos within gold(i) π complexes. Chem. Sci. 2020, 11, 2750–2758. 10.1039/c9sc06398f. PubMed DOI PMC
Zins E.-L.; Pepe C.; Schröder D. Energy-dependent dissociation of benzylpyridinium ions in an ion-trap mass spectrometer. J. Mass Spectrom. 2010, 45, 1253–1260. 10.1002/jms.1847. PubMed DOI
Hanzlová E.; Váňa J.; Shaffer C. J.; Roithová J.; Martinů T. Evidence for the Cyclic CN2 Carbene in the Gas Phase. Org. Lett. 2014, 16, 5482–5485. 10.1021/ol5027602. PubMed DOI
Škríba A.; Schulz J.; Roithová J. Monitoring of Reaction Intermediates in the Gas Phase: Ruthenium-Catalyzed C–C Coupling. Organometallics 2014, 33, 6868–6878. 10.1021/om500933w. DOI
Hývl J.; Roithová J. Mass Spectrometric Studies of Reductive Elimination from Pd(IV) Complexes. Org. Lett. 2014, 16, 200–203. 10.1021/ol403190g. PubMed DOI
Frisch M. J.; Trucks G. W.; Schlegel H. B.; Scuseria G. E.; Robb M. A.; Cheeseman J. R.; Scalmani G.; Barone V.; Mennucci B.; Petersson G. A.; Nakatsuji H.; Caricato M.; Li X.; Hratchian H. P.; Izmaylov A. F.; Bloino J.; Zheng G.; Sonnenberg J. L.; Hada M.; Ehara M.; Toyota K.; Fukuda R.; Hasegawa J.; Ishida M.; Nakajima T.; Honda Y.; Kitao O.; Nakai H.; Vreven T.; Montgomery J. A. Jr.; Peralta J. E.; Ogliaro F.; Bearpark M. J.; Heyd J.; Brothers E. N.; Kudin K. N.; Staroverov V. N.; Kobayashi R.; Normand J.; Raghavachari K.; Rendell A. P.; Burant J. C.; Iyengar S. S.; Tomasi J.; Cossi M.; Rega N.; Millam N. J.; Klene M.; Knox J. E.; Cross J. B.; Bakken V.; Adamo C.; Jaramillo J.; Gomperts R.; Stratmann R. E.; Yazyev O.; Austin A. J.; Cammi R.; Pomelli C.; Ochterski J. W.; Martin R. L.; Morokuma K.; Zakrzewski V. G.; Voth G. A.; Salvador P.; Dannenberg J. J.; Dapprich S.; Daniels A. D.; Farkas Ö.; Foresman J. B.; Ortiz J. V.; Cioslowski J.; Fox D. J.. Gaussian 09; Gaussian, Inc.: Wallingford, CT, USA, 2009.
Adamo C.; Barone V. Exchange functionals with improved long-range behavior and adiabatic connection methods without adjustable parameters: The mPW and mPW1PW models. J. Chem. Phys. 1998, 108, 664–675. 10.1063/1.475428. DOI
Dunning T. H. Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen. J. Chem. Phys. 1989, 90, 1007–1023. 10.1063/1.456153. DOI
Hay P. J.; Wadt W. R. Ab initio effective core potentials for molecular calculations. Potentials for K to Au including the outermost core orbitals. J. Chem. Phys. 1985, 82, 299–310. 10.1063/1.448975. DOI
Simon S.; Duran M.; Dannenberg J. J. How does basis set superposition error change the potential surfaces for hydrogen-bonded dimers?. J. Chem. Phys. 1996, 105, 11024–11031. 10.1063/1.472902. DOI
Reed A. E.; Weinstock R. B.; Weinhold F. Natural population analysis. J. Chem. Phys. 1985, 83, 735–746. 10.1063/1.449486. DOI
Zhao Y.; Truhlar D. G. Density Functionals with Broad Applicability in Chemistry. Acc. Chem. Res. 2008, 41, 157–167. 10.1021/ar700111a. PubMed DOI
Jašík J.; Žabka J.; Roithová J.; Gerlich D. Infrared spectroscopy of trapped molecular dications below 4K. Int. J. Mass Spectrom. 2013, 354–355, 204–210. 10.1016/j.ijms.2013.06.007. DOI
Barnett N. J.; Slipchenko L. V.; Gordon M. S. The Binding of Ag+ and Au+ to Ethene. J. Phys. Chem. A 2009, 113, 7474–7481. 10.1021/jp900372d. PubMed DOI
Dias H. V. R.; Flores J. A.; Wu J.; Kroll P. Monomeric Copper(I), Silver(I), and Gold(I) Alkyne Complexes and the Coinage Metal Family Group Trends. J. Am. Chem. Soc. 2009, 131, 11249–11255. 10.1021/ja904232v. PubMed DOI
Gabelica V.; Pauw E. D. Internal energy and fragmentation of ions produced in electrospray sources. Mass Spectrom. Rev. 2005, 24, 566–587. 10.1002/mas.20027. PubMed DOI
Di Marco V. B.; Bombi G. G. Electrospray mass spectrometry (ESI-MS) in the study of metal–ligand solution equilibria. Mass Spectrom. Rev. 2006, 25, 347–379. 10.1002/mas.20070. PubMed DOI
Suresh C. H.; Koga N. Quantifying the Electronic Effect of Substituted Phosphine Ligands via Molecular Electrostatic Potential. Inorg. Chem. 2002, 41, 1573–1578. 10.1021/ic0109400. PubMed DOI
Gatineau D.; Lesage D.; Clavier H.; Dossmann H.; Chan C. H.; Milet A.; Memboeuf A.; Cole R. B.; Gimbert Y. Bond dissociation energies of carbonyl gold complexes: a new descriptor of ligand effects in gold(i) complexes?. Dalton Trans. 2018, 47, 15497–15505. 10.1039/c8dt03721c. PubMed DOI
Dias H. V. R.; Dash C.; Yousufuddin M.; Celik M. A.; Frenking G. Cationic Gold Carbonyl Complex on a Phosphine Support. Inorg. Chem. 2011, 50, 4253–4255. 10.1021/ic200757j. PubMed DOI
Bayler A.; Schier A.; Bowmaker G. A.; Schmidbaur H. Gold Is Smaller than Silver. Crystal Structures of [Bis(trimesitylphosphine)gold(I)] and [Bis(trimesitylphosphine)silver(I)] Tetrafluoroborate. J. Am. Chem. Soc. 1996, 118, 7006–7007. 10.1021/ja961363v. DOI
Roithová J. Characterization of reaction intermediates by ion spectroscopy. Chem. Soc. Rev. 2012, 41, 547–559. 10.1039/c1cs15133a. PubMed DOI
Roithová J.; Gray A.; Andris E.; Jašík J.; Gerlich D. Helium Tagging Infrared Photodissociation Spectroscopy of Reactive Ions. Acc. Chem. Res. 2016, 49, 223–230. 10.1021/acs.accounts.5b00489. PubMed DOI
Jašíková L.; Roithová J. Infrared Multiphoton Dissociation Spectroscopy with Free-Electron Lasers: On the Road from Small Molecules to Biomolecules. Chem.—Eur. J. 2018, 24, 3374–3390. 10.1002/chem.201705692. PubMed DOI
Škríba A.; Jašík J.; Andris E.; Roithová J. Interaction of Ruthenium(II) with Terminal Alkynes: Benchmarking DFT Methods with Spectroscopic Data. Organometallics 2016, 35, 990–994. 10.1021/acs.organomet.6b00021. DOI
Schmidbaur H.; Schier A. Gold η2-Coordination to Unsaturated and Aromatic Hydrocarbons: The Key Step in Gold-Catalyzed Organic Transformations. Organometallics 2010, 29, 2–23. 10.1021/om900900u. DOI
Nechaev M. S.; Rayón V. M.; Frenking G. Energy Partitioning Analysis of the Bonding in Ethylene and Acetylene Complexes of Group 6, 8, and 11 Metals: (CO)5TM–C2Hx and Cl4TM–C2Hx (TM = Cr, Mo, W), (CO)4TM–C2Hx (TM = Fe, Ru, Os), and TM+–C2Hx (TM = Cu, Ag, Au). J. Phys. Chem. A 2004, 108, 3134–3142. 10.1021/jp031185+. DOI
Ziegler T.; Rauk A. A theoretical study of the ethylene-metal bond in complexes between copper(1+), silver(1+), gold(1+), platinum(0) or platinum(2+) and ethylene, based on the Hartree-Fock-Slater transition-state method. Inorg. Chem. 1979, 18, 1558–1565. 10.1021/ic50196a034. DOI
Lu Z.; Li T.; Mudshinge S. R.; Xu B.; Hammond G. B. Optimization of Catalysts and Conditions in Gold(I) Catalysis—Counterion and Additive Effects. Chem. Rev. 2021, 10.1021/acs.chemrev.0c00713. PubMed DOI