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The coordination chemistry of the ligand isotopologues (including the NA derivative) was investigated with the paramagnetic lanthanides Ce and Nd and the paramagnetic actinide elements Np and Pu, furnishing\n                    <jats:bold>\n                      MI(\n                      <jats:sup>Ar<\/jats:sup>\n                      BiAMP\n                      <jats:italic>\n                        <jats:sup>t<\/jats:sup>\n                      <\/jats:italic>\n                      <jats:sup>Bu<\/jats:sup>\n                      )(thf)\n                      <jats:sub>3<\/jats:sub>\n                    <\/jats:bold>\n                    (M = Ce(\n                    <jats:bold>1<\/jats:bold>\n                    ), Nd(\n                    <jats:bold>2<\/jats:bold>\n                    ), Np(\n                    <jats:bold>3<\/jats:bold>\n                    ), Pu(\n                    <jats:bold>4<\/jats:bold>\n                    )),\n                    <jats:bold>\n                      MI(\n                      <jats:italic>d<\/jats:italic>\n                      <jats:sub>4<\/jats:sub>\n                      \u2010\n                      <jats:sup>Ar<\/jats:sup>\n                      BiAMP\n                      <jats:italic>\n                        <jats:sup>t<\/jats:sup>\n                      <\/jats:italic>\n                      <jats:sup>Bu<\/jats:sup>\n                      )(thf)\n                      <jats:sub>3<\/jats:sub>\n                    <\/jats:bold>\n                    (M = Ce(\n                    <jats:bold>\n                      <jats:sup>2<\/jats:sup>\n                      H\u20101\n                    <\/jats:bold>\n                    ), Nd(\n                    <jats:bold>\n                      <jats:sup>2<\/jats:sup>\n                      H\u20102\n                    <\/jats:bold>\n                    )) and\n                    <jats:bold>\n                      MI(\n                      <jats:sup>13<\/jats:sup>\n                      C\n                      <jats:sub>2<\/jats:sub>\n                      \u2010\n                      <jats:sup>Ar<\/jats:sup>\n                      BiAMP\n                      <jats:italic>\n                        <jats:sup>t<\/jats:sup>\n                      <\/jats:italic>\n                      <jats:sup>Bu<\/jats:sup>\n                      )(thf)\n                      <jats:sub>3<\/jats:sub>\n                    <\/jats:bold>\n                    (M = Ce(\n                    <jats:bold>\n                      <jats:sup>13<\/jats:sup>\n                      C\u20101\n                    <\/jats:bold>\n                    ), Nd(\n                    <jats:bold>\n                      <jats:sup>13<\/jats:sup>\n                      C\u20102\n                    <\/jats:bold>\n                    ), Np(\n                    <jats:bold>\n                      <jats:sup>13<\/jats:sup>\n                      C\u20103\n                    <\/jats:bold>\n                    ), Pu(\n                    <jats:bold>\n                      <jats:sup>13<\/jats:sup>\n                      C\u20104\n                    <\/jats:bold>\n                    )); each complex bears the metal in the 3+ oxidation state chelated by the amide groups and phosphorus atom of the\n                    <jats:sup>Ar<\/jats:sup>\n                    BiAMP\n                    <jats:italic>\n                      <jats:sup>t<\/jats:sup>\n                    <\/jats:italic>\n                    <jats:sup>Bu<\/jats:sup>\n                    ligand. Multinuclear (\n                    <jats:sup>1<\/jats:sup>\n                    H,\n                    <jats:sup>31<\/jats:sup>\n                    P,\n                    <jats:sup>13<\/jats:sup>\n                    C, and\n                    <jats:sup>2<\/jats:sup>\n                    H) NMR characterization of the complexes revealed wide windows of paramagnetically shifted resonances; the isotopically enriched derivatives allowed for the unambiguous identification of the methylene environments, highlighting the utility of the\n                    <jats:bold>\n                      <jats:sup>Ar<\/jats:sup>\n                      BiAMP\n                      <jats:italic>\n                        <jats:sup>t<\/jats:sup>\n                      <\/jats:italic>\n                      <jats:sup>Bu<\/jats:sup>\n                    <\/jats:bold>\n                    ligands for providing rich spectroscopic signatures of paramagnetic\n                    <jats:italic>f<\/jats:italic>\n                    \u2010element coordination complexes. A combination of single\u2010crystal X\u2010ray diffraction and UV\u2010vis\u2010NIR spectroscopic techniques was also employed for the characterization of the compounds. Actinide complexes\n                    <jats:bold>3<\/jats:bold>\n                    and\n                    <jats:bold>4<\/jats:bold>\n                    possess rare examples of molecular transuranium element\u2013phosphorus bonds and the first examples of transuranium element\u2013phosphine interactions.\n                  <\/jats:p>","DOI":"10.1002\/advs.78113","type":"journal-article","created":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T16:14:17Z","timestamp":1791130457000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Phosphine Coordination to Ce, Nd, Np, and Pu in\n                    <sup>Ar<\/sup>\n                    BiAMP\n                    <i>\n                      <sup>t<\/sup>\n                    <\/i>\n                    <sup>Bu<\/sup>\n                    \u2010Supported Complexes and Their\n                    <sup>2<\/sup>\n                    H and\n                    <sup>13<\/sup>\n                    C Isotopologues"],"prefix":"10.1002","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3607-4063","authenticated-orcid":false,"given":"Novan A. 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