{"id":19,"date":"2022-07-01T14:57:17","date_gmt":"2022-07-01T18:57:17","guid":{"rendered":"https:\/\/sites.bu.edu\/cueny-group\/?page_id=19"},"modified":"2026-07-23T20:09:54","modified_gmt":"2026-07-24T00:09:54","slug":"publications","status":"publish","type":"page","link":"https:\/\/sites.bu.edu\/cueny-group\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"

(15) Banerjee, S.; Blakemore, J.; Brown, C.; Bonitatibus, P.; Campbell, B.; Carsch, K.; Chambers, M.; Cueny, E.<\/strong>; Dempsey, J.; Diaconescu, P.; Dobereiner, G.; Duletski, O.; Flinkingshelt, F.; Ghosh, A.; Gorden, A.; Gordon, J.; Gordon, J.; Hazari, N.; Heiden, Z.; Hokanson, S.; Javier-Jim\u00e9nez, D.; Kannangara, P.; Klosin, J.; Laitar, D.; LaPointe, A.; Lee, S.; L\u00e9onard, N.; Liberman-Martin, A.; Machan, C.; Mane, E.; McCormick, T.; Mu, N.; Nett, A.; Olarinde, O.; Orzolek, B.; Pham, A.-T.; Plodukhin, A.; Radlauer, M.; Raffman, E.; Roberts, C.; Sadow, A.; Sampson, J.; Stanley, G.; Alexandra, A.; Strong, C.; Tonzetich, Z.; Trovitch, R.; Yadav, V.; Warren, T.; Waterman, R., Reproducibility, Replicability, and Research Quality in Homogeneous Catalysis
\nChemRxiv<\/em> 2026<\/strong>
\n10.26434\/chemrxiv.15004014\/v1<\/a><\/span><\/p>\n

(15) Luna, S., Jr.; Skipper, H. E.; Lawson, B.; Cueny, E.; Kamenetska, M.* Metallophilicity Enhances Electron Transport through Parallel Organometallic 1D Chains Formed in Situ
\nJ. Am. Chem. Soc.<\/em> 2026<\/strong>, 148<\/i>, 8961-8969
\n10.1021\/jacs.5c21701<\/a>
\n\"\"
\n<\/span><\/p>\n

(14) Farmer-Mason, K. M.; Bacon, J. W.; Cueny, E. S.<\/strong>* Stability of metal\u2013metal interactions in dinuclear Pt\u2013Au complexes as a function of bridging Pt\u2013arene ring electronics
\nDalton Trans.<\/em> 2025<\/strong>, 54<\/em>\u200b, 16241-16253
\n10.1039\/d5dt02048d<\/a>
\n\"\"
\n<\/span><\/p>\n

(13) Marghalani, R.; Gibson, V.; Bacon, J. W.; Cueny, E. S.<\/strong>* Multinuclear Pt\u2013Ag Complexes: How Pt\u2013Arene Ring Electronics Influences Structure
\n<\/span>Journal of Coordination Chemistry<\/em>, 2025<\/strong>, 78<\/em>, 2515-2525<\/span>
\n<\/i>10.1080\/00958972.2025.2517660<\/a>
\nInvited submission to the Emerging Leaders in Coordination Chemistry Special Issue<\/em>
\n\"\"<\/i><\/p>\n

(12) Marghalani, R.; Cueny, E. S.<\/strong>* Stability of Metal\u2013Metal Interactions in Transmetallation Intermediates Based on Electronics of Bridging Arene Ligands Determined Through Pyridine Titrations
\nDalton Trans.<\/em> 2024<\/strong>, 53<\/em>\u200b, 18839-18844
\n<\/span>10.1039\/D4DT01828A<\/a>
\nInvited submission to the New Talent: Americas Special Issue<\/em><\/p>\n

\"\"<\/p>\n

(11) <\/span>Cueny, E. S.<\/strong>*\u00a0<\/span>Chromophore Quench Labeling: Simulated Snapshots of Molar Mass Distributions for the Rapid Mechanistic Analysis of Catalytic Alkene Polymerization<\/span>
\n<\/span>ACS Catal.<\/em>,\u00a0<\/span>2022<\/strong>,<\/span>\u00a012<\/em>\u200b, 1117-1127<\/span>
\n10.1021\/acscatal.1c04614<\/a><\/p>\n

\"\"<\/p>\n

Prior to Boston University<\/em>
\n<\/strong><\/p>\n

(10) McDaniel, T.; Smith, N. E.; Cueny, E. S.<\/strong>; Landis, C. R. Dual-Chain Polymerization at an Early Transition-Metal Single-Site Catalyst ACS Catal.<\/em> 2022<\/strong>, 12<\/em>, 10680-10689
\n10.1021\/acscatal.2c01240<\/a><\/p>\n

(9)\u00a0<\/span>Cueny, E. S.<\/strong>; Nieszala, M. R.; Froese, R. D. J.; Landis, C. R.* Nature of the Active Catalyst in the Hafnium-Pyridyl Amido-Catalyzed Alkene Polymerization\u00a0<\/span>ACS Catal.<\/em>,\u00a0<\/span>2021<\/strong>,<\/span>\u00a0<\/span>11<\/em>, 4301-4309<\/span>
\n10.1021\/acscatal.1c00394<\/a>
\n\u200b<\/span>
\n(8)\u00a0<\/span>Cueny, E. S.<\/strong>; Sita, L. R.; Landis, C. R.* Quantitative Validation of the Living Coordinative Chain Transfer Polymerization of 1-Hexene using Chromophore Quench-Labeling\u00a0<\/span>Macromolecules<\/em>,\u00a0<\/span>2020<\/strong>,<\/span>\u00a0<\/span>53<\/em>, 5816-5825<\/span>
\n10.1021\/acs.macromol.0c00552<\/a><\/p>\n

(7)\u00a0<\/span>Cueny, E. S.<\/strong>; Landis, C. R.* The Hafnium-Pyridyl Amido-Catalyzed Copolymerization of Ethylene and 1-Octene: How Small Amounts of Ethylene Impact Catalysis\u00a0<\/span>ACS Catal.<\/em>,\u00a0<\/span>2019<\/strong>,\u00a0<\/span>9<\/em>, 3338-3348<\/span>
\n10.1021\/acscatal.9b00250<\/a><\/p>\n

(6)\u00a0<\/span>Cueny, E. S.<\/strong>; Landis, C. R.* Zinc-Mediated Chain Transfer from Hafnium to Aluminum in the Hafnium-Pyridyl Amido-Catalyzed 1-Octene Polymerization Revealed Through Job Plot Analysis\u00a0<\/span>Organometallics,\u00a0<\/span><\/em>2019<\/strong>, 38<\/em>, 926-932<\/span>
\nACS Editor\u2019s Choice<\/em><\/strong>
\n10.1021\/acs.organomet.8b00900<\/a><\/p>\n

(5)\u00a0<\/span>Cueny, E. S.<\/strong>; Johnson, H. C.; Landis, C. R.* Chain Transfer Using Trialkyl-Aluminum Reagents in the Hafnium Pyridyl-Amido-Catalyzed Polymerization of 1-Octene\u00a0<\/span>ACS Catal.,\u00a0<\/span><\/em>2018<\/strong>,\u00a0<\/span>8<\/em>, 11605-11614<\/span>
\n10.1021\/acscatal.8b03615<\/a><\/p>\n

(4) Johnson, H. C.;\u00a0<\/span>Cueny, E. S.<\/strong>; Landis, C. R.* Chain Transfer with Dialkyl Zinc During Hafnium-Pyridyl Amido-Catalyzed Polymerization of 1-Octene: Relative Rates, Reversibility and Kinetic Models\u00a0<\/span>ACS Catal.<\/em>,\u00a0<\/span>2018<\/strong>,\u00a0<\/span>8<\/em>, 4178-4188<\/span>
\n10.1021\/acscatal.8b00524<\/a><\/p>\n

(3)\u00a0<\/span>Cueny, E. S.<\/strong>;\u2020 Johnson, H. C.;\u2020 Anding, B. J.; Landis, C. R.* Mechanistic Studies of Hafnium-Pyridyl Amido Catalyzed 1-Octene Polymerization and Chain Transfer Using Quench-Labeling Methods\u00a0<\/span>J. Am. Chem. Soc.<\/em>,\u00a0<\/span>2017<\/strong>,\u00a0<\/span>139<\/em>, 11903-11912<\/span>
\n10.1021\/jacs.7b05729<\/a><\/p>\n

(2) Respondek, T.; Sharma, R.; Herroon, M. K.; Garner, R. N.; Knoll, J. D.;\u00a0<\/span>Cueny, E.<\/strong>; Turro, C.; Podgorski, I.; Kodanko, J. J.* Inhibition of Cathepsin Activity in a Cell-Based Assay by a Light-Activated Ruthenium Compound\u00a0<\/span>ChemMedChem,<\/em>\u00a0<\/span>2014<\/strong>,\u00a0<\/span>9<\/em>, 1306-1315<\/span>
\n10.1002\/cmdc.201400081<\/a><\/p>\n

(1) Respondek T.;\u00a0<\/span>Cueny E.<\/strong>; Kodanko J. J.* Cumyl Ester as the C-Terminal Protecting Group in the Enantioselective Alkylation of Glycine Benzophenone Imine\u00a0<\/span>Org. Lett.<\/em>\u00a0<\/span>2012<\/strong>,\u00a0<\/span>14<\/em>, 150\u2013153<\/span>
\n10.1021\/ol202939g<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

(15) Banerjee, S.; Blakemore, J.; Brown, C.; Bonitatibus, P.; Campbell, B.; Carsch, K.; Chambers, M.; Cueny, E.; Dempsey, J.; Diaconescu, P.; Dobereiner, G.; Duletski, O.; Flinkingshelt, F.; Ghosh, A.; Gorden, A.; Gordon, J.; Gordon, J.; Hazari, N.; Heiden, Z.; Hokanson, S.; Javier-Jim\u00e9nez, D.; Kannangara, P.; Klosin, J.; Laitar, D.; LaPointe, A.; Lee, S.; L\u00e9onard, N.; […]<\/p>\n","protected":false},"author":21105,"featured_media":0,"parent":0,"menu_order":3,"comment_status":"closed","ping_status":"closed","template":"page-templates\/no-sidebars.php","meta":[],"_links":{"self":[{"href":"https:\/\/sites.bu.edu\/cueny-group\/wp-json\/wp\/v2\/pages\/19"}],"collection":[{"href":"https:\/\/sites.bu.edu\/cueny-group\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/sites.bu.edu\/cueny-group\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/sites.bu.edu\/cueny-group\/wp-json\/wp\/v2\/users\/21105"}],"replies":[{"embeddable":true,"href":"https:\/\/sites.bu.edu\/cueny-group\/wp-json\/wp\/v2\/comments?post=19"}],"version-history":[{"count":17,"href":"https:\/\/sites.bu.edu\/cueny-group\/wp-json\/wp\/v2\/pages\/19\/revisions"}],"predecessor-version":[{"id":124,"href":"https:\/\/sites.bu.edu\/cueny-group\/wp-json\/wp\/v2\/pages\/19\/revisions\/124"}],"wp:attachment":[{"href":"https:\/\/sites.bu.edu\/cueny-group\/wp-json\/wp\/v2\/media?parent=19"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}