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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">109</journal-id>
      <journal-id journal-id-type="index">urn:lsid:arphahub.com:pub:3dc5f44e-8666-58db-bc76-a455210e8891</journal-id>
      <journal-title-group>
        <journal-title xml:lang="en">JUCS - Journal of Universal Computer Science</journal-title>
        <abbrev-journal-title xml:lang="en">jucs</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0948-695X</issn>
      <issn pub-type="epub">0948-6968</issn>
      <publisher>
        <publisher-name>Journal of Universal Computer Science</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.3217/jucs-013-11-1514</article-id>
      <article-id pub-id-type="publisher-id">28878</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Research Article</subject>
        </subj-group>
        <subj-group subj-group-type="scientific_subject">
          <subject>G.2.2 - Graph Theory</subject>
          <subject>J.2 - PHYSICAL SCIENCES AND ENGINEERING</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Perfect Matchings in Polyhexes, or Recent Graph-theoretical Contributions to Benzenoids</article-title>
      </title-group>
      <contrib-group content-type="authors">
        <contrib contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Balaban</surname>
            <given-names>Alexandru T.</given-names>
          </name>
          <email xlink:type="simple">balabana@tamug.edu</email>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Randić</surname>
            <given-names>Milan</given-names>
          </name>
          <xref ref-type="aff" rid="A2">2</xref>
        </contrib>
      </contrib-group>
      <aff id="A1">
        <label>1</label>
        <addr-line content-type="verbatim">Texas A&amp;M University at Galveston, Galveston, United States of America</addr-line>
        <institution>Texas A&amp;M University at Galveston</institution>
        <addr-line content-type="city">Galveston</addr-line>
        <country>United States of America</country>
      </aff>
      <aff id="A2">
        <label>2</label>
        <addr-line content-type="verbatim">National Institute of Chemistry, Ljubljana, Slovenia</addr-line>
        <institution>National Institute of Chemistry</institution>
        <addr-line content-type="city">Ljubljana</addr-line>
        <country>Slovenia</country>
      </aff>
      <author-notes>
        <fn fn-type="corresp">
          <p>Corresponding author: Alexandru T. Balaban (<email xlink:type="simple">balabana@tamug.edu</email>).</p>
        </fn>
        <fn fn-type="edited-by">
          <p>Academic editor: </p>
        </fn>
      </author-notes>
      <pub-date pub-type="collection">
        <year>2007</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>28</day>
        <month>11</month>
        <year>2007</year>
      </pub-date>
      <volume>13</volume>
      <issue>11</issue>
      <fpage>1514</fpage>
      <lpage>1539</lpage>
      <uri content-type="arpha" xlink:href="http://openbiodiv.net/A12A2F2A-8048-5A03-8950-2CF54030FC43">A12A2F2A-8048-5A03-8950-2CF54030FC43</uri>
      <uri content-type="zenodo_dep_id" xlink:href="https://zenodo.org/record/6999970">6999970</uri>
      <permissions>
        <copyright-statement>Alexandru T. Balaban, Milan Randić</copyright-statement>
        <license license-type="creative-commons-attribution" xlink:href="" xlink:type="simple">
          <license-p>This article is freely available under the J.UCS Open Content License.</license-p>
        </license>
      </permissions>
      <abstract>
        <label>Abstract</label>
        <p>After an introduction on the history of polycyclic aromatic compounds, recent advances in the theory of benzenoids are briefly reviewed. Then using systems with 4, 5, or 6 benzenoid rings for illustration, the partition of the P π-electrons among the rings of the benzenoid is presented, followed by a different way of examining the distribution of these π-electrons which is called the signature of the benzenoid, consisting in six integers from s6 to s1. The P π-electrons are divided between the two sums s6 + s5 + s2 + s1 and s4 + s3 characterizing thereby the closeness of benzenoids to all-resonant structures according to Clars theory.</p>
      </abstract>
    </article-meta>
  </front>
</article>
