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<article article-type="research-article">
  <front>
    <journal-meta>
      <journal-id journal-id-type="aggregator">72010410</journal-id>
      <journal-title>NIP &amp; Digital Fabrication Conference</journal-title>
      <abbrev-journal-title>nip digi fabric conf</abbrev-journal-title>
      <issn pub-type="ppub">2169-4451</issn><issn pub-type="epub"/>
      <publisher>
        <publisher-name>Society of Imaging Science and Technology</publisher-name>
        <publisher-loc>7003 Kilworth Lane, Springfield, VA 22151, USA</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta><article-id pub-id-type="doi">10.2352/ISSN.2169-4451.2004.20.1.art00002_2</article-id>
      <article-id pub-id-type="sici">2169-4451(20040101)2004:2L.520;1-</article-id>
      <article-id pub-id-type="publisher-id">nip_v2004n2/splitsection2.xml</article-id>
      <article-id pub-id-type="other">/ist/nipdf/2004/00002004/00000002/art00002</article-id>
      <article-categories>
        <subj-group>
          <subject>Articles</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Polymorph of 1,4-diketo-3,6-dipyridyl&#x2013;pyrrolo-[3,4-c]pyrrole</article-title>
      </title-group>
      <contrib-group>
        <contrib>
          <name>
            <surname>Imoda</surname>
            <given-names>Tomohiko</given-names>
          </name>
        </contrib>
        <contrib>
          <name>
            <surname>Takahashi</surname>
            <given-names>Hiroo</given-names>
          </name>
        </contrib>
        <contrib>
          <name>
            <surname>Mizuguchi</surname>
            <given-names>Jin</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date>
        <day>01</day>
        <month>01</month>
        <year>2004</year>
      </pub-date>
      <volume>2004</volume>
      <issue>2</issue>
      <fpage>520</fpage>
      <lpage>523</lpage>
      <permissions>
        <copyright-year>2004</copyright-year>
      </permissions>
      <abstract>
        <p>Diketopyrrolopyrroles (DPP) are well-known organic pigments. The title compound (DPPP) is one of DPP derivatives that shows a high proton affinity because of the N atoms of the pyridyl ring. Protonation at the N-site brings about a variety of changes in color as well as in electrical
 and photoelectrical conductivities. Two crystal modifications have been found to exist: DPPP I (grown from vapor phase) and DPPP II (grown from solution). Structure analysis revealed that there is a striking difference in intermolecular hydrogen bonds between two modifications: DPPP I is characterized
 only by NH&#x2026;O hydrogen bonds whereas DPPP II include two of the H-bond based on NH&#x2026;N and NH&#x2026;O.</p>
      </abstract>
    </article-meta>
  </front>
</article>
