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<titleInfo><title>Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design</title></titleInfo>


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<name type="personal">
  <namePart type="given">Julie A.</namePart>
  <namePart type="family">Peterson</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Friedrich J</namePart>
  <namePart type="family">Stricker</namePart>
  <role><roleTerm type="text">author</roleTerm> </role><identifier type="local">7aca2cfc-46cf-11f0-abd3-8c96b5186745</identifier></name>
<name type="personal">
  <namePart type="given">Javier</namePart>
  <namePart type="family">Read de Alaniz</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>














<abstract lang="eng">DFT calculations were used to find an optimal substitution site on the triene backbone of a donor–acceptor Stenhouse adduct photoswitch to tune the equillibrium and switching kinetics of DASA without modifying the donor and acceptor groups. Using this approach we demonstrate a new means to tuning DASA based photoswitches by increasing the energy of the closed form relative to the open form. To highlight the potential of this approach a new DASA derivative bearing a methyl substituent on the 5-position of the triene was synthesized and the effect of this substitution was studied using 1H NMR spectroscopy, time-dependent UV-Vis and solvatochromic analysis. The new DASA derivative shows a higher dark equillibrium, favoring the open form, and drastically faster thermal recovery than the unsubstituted derivative with the same donor and acceptor.</abstract>

<originInfo><publisher>Royal Society of Chemistry</publisher><dateIssued encoding="w3cdtf">2022</dateIssued>
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<language><languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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<relatedItem type="host"><titleInfo><title>Chemical Communications</title></titleInfo>
  <identifier type="issn">1359-7345</identifier>
  <identifier type="eIssn">1364-548X</identifier>
  <identifier type="MEDLINE">35075464</identifier><identifier type="doi">10.1039/d1cc06235b</identifier>
<part><detail type="volume"><number>58</number></detail><detail type="issue"><number>14</number></detail><extent unit="pages">2303-2306</extent>
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<ieee>J. A. Peterson, F. J. Stricker, and J. Read de Alaniz, “Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design,” &lt;i&gt;Chemical Communications&lt;/i&gt;, vol. 58, no. 14. Royal Society of Chemistry, pp. 2303–2306, 2022.</ieee>
<ista>Peterson JA, Stricker FJ, Read de Alaniz J. 2022. Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design. Chemical Communications. 58(14), 2303–2306.</ista>
<chicago>Peterson, Julie A., Friedrich J Stricker, and Javier Read de Alaniz. “Improving the Kinetics and Dark Equilibrium of Donor-Acceptor Stenhouse Adduct by Triene Backbone Design.” &lt;i&gt;Chemical Communications&lt;/i&gt;. Royal Society of Chemistry, 2022. &lt;a href=&quot;https://doi.org/10.1039/d1cc06235b&quot;&gt;https://doi.org/10.1039/d1cc06235b&lt;/a&gt;.</chicago>
<mla>Peterson, Julie A., et al. “Improving the Kinetics and Dark Equilibrium of Donor-Acceptor Stenhouse Adduct by Triene Backbone Design.” &lt;i&gt;Chemical Communications&lt;/i&gt;, vol. 58, no. 14, Royal Society of Chemistry, 2022, pp. 2303–06, doi:&lt;a href=&quot;https://doi.org/10.1039/d1cc06235b&quot;&gt;10.1039/d1cc06235b&lt;/a&gt;.</mla>
<ama>Peterson JA, Stricker FJ, Read de Alaniz J. Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design. &lt;i&gt;Chemical Communications&lt;/i&gt;. 2022;58(14):2303-2306. doi:&lt;a href=&quot;https://doi.org/10.1039/d1cc06235b&quot;&gt;10.1039/d1cc06235b&lt;/a&gt;</ama>
<short>J.A. Peterson, F.J. Stricker, J. Read de Alaniz, Chemical Communications 58 (2022) 2303–2306.</short>
<apa>Peterson, J. A., Stricker, F. J., &amp;#38; Read de Alaniz, J. (2022). Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design. &lt;i&gt;Chemical Communications&lt;/i&gt;. Royal Society of Chemistry. &lt;a href=&quot;https://doi.org/10.1039/d1cc06235b&quot;&gt;https://doi.org/10.1039/d1cc06235b&lt;/a&gt;</apa>
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