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              <p>This study reports the isolation and the structural (X-ray), UV−vis, and NMR characterization of a series of electron-rich Ru(II) acetylide complexes of the formula (η2-dppe)(η5-C5Me5)Ru(CC)-1,4-(C6H4)X (1a−f; X = NO2, CN, F, H, OMe, NH2) and (η2-dppe)(η5-C5Me5)Ru(CC)-1,3-(C6H4)F (1c-m), as well as the spectroscopic (near-IR and ESR) in situ characterization of the corresponding elusive Ru(III) radical cations. The spectroscopic data are discussed in connection with DFT computations, and a consistent picture of the electronic structure of these Ru(II) and Ru(III) acetylide complexes is proposed. Notably, the strong reactivity of the Ru(III) radicals evidenced in this contribution constitutes a major difference with the relative stability of the known iron analogues.</p>
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            <ref type="url">http://www.insa-rennes.fr/</ref>
          </desc>
          <listRelation>
            <relation active="#struct-301232" type="direct"/>
          </listRelation>
        </org>
        <org type="regroupinstitution" xml:id="struct-301232" status="VALID">
          <idno type="IdRef">162105150</idno>
          <orgName>Institut National des Sciences Appliquées</orgName>
          <orgName type="acronym">INSA</orgName>
          <desc>
            <address>
              <country key="FR"/>
            </address>
          </desc>
        </org>
        <org type="institution" xml:id="struct-300373" status="VALID">
          <idno type="ROR">https://ror.org/01h0ffh48</idno>
          <orgName>Ecole Nationale Supérieure de Chimie de Rennes</orgName>
          <orgName type="acronym">ENSCR</orgName>
          <desc>
            <address>
              <country key="FR"/>
            </address>
          </desc>
        </org>
      </listOrg>
    </back>
  </text>
</TEI>