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        <datestamp>2026-09-29T04:03:58Z</datestamp>
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        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>A Phosphotungstate
Catalyst with Both Brønsted
and Lewis Acid Sites for Synthesis of Bis(indolyl)methane Derivatives</dc:title>
          <dc:creator>Miao Zhang (17216)</dc:creator>
          <dc:creator>Lin Chen (54305)</dc:creator>
          <dc:creator>Chizhao Song (24455302)</dc:creator>
          <dc:creator>Bing Yan (170259)</dc:creator>
          <dc:creator>Lin Sun (105539)</dc:creator>
          <dc:creator>Qiuxia Han (1791697)</dc:creator>
          <dc:creator>Pengtao Ma (779212)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Sociology</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>reaction proceeds efficiently</dc:subject>
          <dc:subject>possible catalytic mechanism</dc:subject>
          <dc:subject>new catalytic strategies</dc:subject>
          <dc:subject>lewis acid sites</dc:subject>
          <dc:subject>electrophilic substitution reaction</dc:subject>
          <dc:subject>attracted increasing attention</dc:subject>
          <dc:subject>phosphotungstate [( ch</dc:subject>
          <dc:subject>room temperature without</dc:subject>
          <dc:subject>9 &lt;/ sub</dc:subject>
          <dc:subject>2 &lt;/ sub</dc:subject>
          <dc:subject>room temperature</dc:subject>
          <dc:subject>yielding reactions</dc:subject>
          <dc:subject>thereby expanding</dc:subject>
          <dc:subject>synthetic scope</dc:subject>
          <dc:subject>synthesized via</dc:subject>
          <dc:subject>short period</dc:subject>
          <dc:subject>phosphotungstate catalyst</dc:subject>
          <dc:subject>methane derivatives</dc:subject>
          <dc:subject>key method</dc:subject>
          <dc:subject>expanding applications</dc:subject>
          <dc:subject>diarylmethane derivatives</dc:subject>
          <dc:subject>completed within</dc:subject>
          <dc:subject>based compounds</dc:subject>
          <dc:subject>also proposed</dc:subject>
          <dc:subject>(&lt; b</dc:subject>
          <dc:description>The Friedel–Crafts alkylation of indoles with
aldehydes
is a key method for synthesizing bis(indolyl)methanes (BIMs). With
the expanding applications of BIMs in medicine and agriculture, the
development of new catalytic strategies to facilitate their synthesis
has attracted increasing attention. In this study, we report a mild,
cost-effective, and environmentally friendly catalyzed Friedel–Crafts
reaction of indoles with aldehydes. The catalyst, phosphotungstate
[(CH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;NH&lt;sub&gt;2&lt;/sub&gt;]&lt;sub&gt;9&lt;/sub&gt;[Sb&lt;sub&gt;3&lt;/sub&gt;(A-α-PW&lt;sub&gt;9&lt;/sub&gt;O&lt;sub&gt;34&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;]·7H&lt;sub&gt;2&lt;/sub&gt;O (&lt;b&gt;SbPW&lt;/b&gt;), was synthesized via a conventional
aqueous solution method. The reaction proceeds efficiently at room
temperature under solvent-free conditions. Under these conditions,
high-yielding reactions were achieved for the synthesis of diarylmethane
derivatives from a variety of aliphatic and aromatic aldehydes, thereby
expanding the synthetic scope of indole-based compounds. The electrophilic
substitution reaction was completed within a short period at room
temperature without the need for a solvent, and a possible catalytic
mechanism is also proposed.</dc:description>
          <dc:date>2026-09-29T00:00:00Z</dc:date>
          <dc:type>Text</dc:type>
          <dc:type>Journal contribution</dc:type>
          <dc:identifier>10.1021/acs.inorgchem.6c02847.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/journal_contribution/A_Phosphotungstate_Catalyst_with_Both_Br_nsted_and_Lewis_Acid_Sites_for_Synthesis_of_Bis_indolyl_methane_Derivatives/34021069</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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