Počet záznamov: 1  

Arylazoindazole photoswitches

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    $a 10.1021/jacs.6b12585 $2 DOI
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    $a 20170815d2017 m y slo 03 ba
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    $a eng
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    $a Arylazoindazole photoswitches $e facile synthesis and functionalization via SNAr substitution $f Raquel Travieso-Puente ... [et al.]
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    $a A straightforward synthetic route to arylazoindazoles via nucleophilic aromatic substitution is presented. Upon deprotonation of the NH group, a C(6)F(5-)substituted formazan undergoes facile cydization as a result of intermolecular nucleophilic substitution (SNAr). This new class of azo photoswitches containing an indazole five-membered heterocycle shows photochemical isomerization with high fatigue resistance. In addition, the Z-isomers have long thermal half-lives in the dark of up to several days at room temperature. The fluorinated indazole group offers a handle for further functionalization and tuning of its properties, as it is shown to be susceptible to a subsequent, highly selective nucleophilic displacement reaction.
    463
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    $1 001 umb_un_cat*0293229 $1 011 $a 0002-7863 $1 011 $a 1520-5126 $1 200 1 $a Journal of the American Chemical Society $v Vol. 139, no. 9 (2017), pp. 3328-3331 $1 210 $a Washington $c The American Chemical Society $d 2017
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    $3 umb_un_auth*0265014 $a arylazoindazoles
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    $3 umb_un_auth*0265015 $a arylindazoly
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    $3 umb_un_auth*0256817 $a fotoprepínače $X photoswitches
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    $3 umb_un_auth*0265018 $a Chen $b Juan $4 070 $9 14
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    $3 umb_un_auth*0265020 $a Jastrzebski $b Johann T. B. H. $4 070 $9 14
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    $3 umb_un_auth*0265021 $a Otten $b Edwin $4 070 $9 15
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Počet záznamov: 1  

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