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首页> 外文期刊>Journal of Physical Organic Chemistry >Complexation of bis‐crown stilbene with alkali and alkaline‐earth metal cations. Ultrafast excited state dynamics of the stilbene‐viologen analogue charge transfer complex
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Complexation of bis‐crown stilbene with alkali and alkaline‐earth metal cations. Ultrafast excited state dynamics of the stilbene‐viologen analogue charge transfer complex

机译:双冠芪与碱和碱土金属阳离子的络合。 超快激发状态动态的斯蒂替斯 - viologen模拟电荷转移复合物

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Abstract > The complex formation of bis(18‐crown‐6)stilbene ( 1 ) and its supramolecular donor‐acceptor complex with <fi>N</fi> , <fi>N</fi> ′‐bis(ammonioethyl) 1,2‐di(4‐pyridyl)ethylene derivative ( 2 ) with alkali and alkaline‐earth metal perchlorates has been studied using absorption, steady‐state fluorescence, and femtosecond transient absorption spectroscopy. The formation of 1 ?M <fi>n</fi> + and 1 ?(M <fi>n</fi> + ) <sub>2</sub> complexes in acetonitrile was demonstrated. The weak long‐wavelength charge‐transfer absorption band of 1 · 2 completely vanishes upon complexation with metal cations because of disruption of the pseudocyclic structure. The spectroscopic and luminescence parameters, stability constants, and 2‐stage dissociation constants were calculated. The initial stage of a recoordination process was found in the excited complexes 1 ?M + and 1 ?(M + ) <sub>2</sub> (M?=?Li, Na). The pronounced fluorescence quenching of 1 · 2 is explained by very fast back electron transfer ( <fi>τ</fi> <sub>et</sub> ?=?0.397?ps). The structure of complex 1 · 2 was studied by X‐ray diffraction; stacked ( 1 · 2 ) <sub> <fi>m</fi> </sub> polymer in which the components were connected by hydrogen bonding and stacking was </span> <span class="z_kbtn z_kbtnclass hoverxs" style="display: none;">展开▼</span> </div> <div class="translation abstracttxt"> <span class="zhankaihshouqi fivelineshidden" id="abstract"> <span>机译:</span><Abstract Type =“main”> <标题类型=“main”>抽象</ title> > BIS(18-Crown-6)斯蒂莱( 1 </ b>)的复杂形成及其超分子具有<FI> N </ FI>,<FI> N </ FI>'-BIS(氨基乙基)1,2-DI(4-吡啶基)乙烯衍生物( 2 / b>),供体 - 受体复合物已经使用碱和碱土金属高氯酸盐使用吸收,稳态荧光和飞秒瞬态吸收光谱进行了研究。形成 1 </ b>Δm <fi> n </ fi> + </ sup>和 1 </ b>?(m <fi> n </证明了乙腈中的<sub> 2 </ sub>复合物。由于假环结构的破坏,<B> 1 </ B>·<B> 2的弱的长波长电荷转移吸收带,在与金属阳离子的粘结后完全消失。计算光谱和发光参数,稳定性常数和2阶段解离常数。在激发的复合物中发现重新编制过程的初始阶段 1 </ b>Δm + </ sup>和 1 </ b>?(m + </ sup >)<sub> 2 </ sub>(m?=?li,na)。通过非常快的回电子传递(<fi>τ</ fi> <sub> et </ sub>Δ=Δ=? 0.397?PS)。通过X射线衍射研究了复合物的络合物 1· 2 </ b>;堆叠( 1 </ b>· 2 </ b>)<sub> <fi> m </ fi> </ sub>聚合物,其中通过氢键连接和堆叠 </span> <span class="z_kbtn z_kbtnclass hoverxs" style="display: none;">展开▼</span> </div> </div> <div class="record"> <h2 class="all_title" id="enpatent33" >著录项</h2> <ul> <li> <span class="lefttit">来源</span> <div style="width: 86%;vertical-align: text-top;display: inline-block;"> <a href='/journal-foreign-35546/'>《Journal of Physical Organic Chemistry》</a> <b style="margin: 0 2px;">|</b><span>2018年第2期</span><b style="margin: 0 2px;">|</b><span>共10页</span> </div> </li> <li> <div class="author"> <span class="lefttit">作者</span> <p id="fAuthorthree" class="threelineshidden zhankaihshouqi"> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Volchkov Valery V.&option=202" target="_blank" rel="nofollow">Volchkov Valery V.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Rusalov Mikhail V.&option=202" target="_blank" rel="nofollow">Rusalov Mikhail V.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Gostev Fedor E.&option=202" target="_blank" rel="nofollow">Gostev Fedor E.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Shelaev Ivan V.&option=202" target="_blank" rel="nofollow">Shelaev Ivan V.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Nadtochenko Viktor A.&option=202" target="_blank" rel="nofollow">Nadtochenko Viktor A.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Vedernikov Artem I.&option=202" target="_blank" rel="nofollow">Vedernikov Artem I.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Efremova Asya A.&option=202" target="_blank" rel="nofollow">Efremova Asya A.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kuzmina Lyudmila G.&option=202" target="_blank" rel="nofollow">Kuzmina Lyudmila G.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Gromov Sergey P.&option=202" target="_blank" rel="nofollow">Gromov Sergey P.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Alfimov Michael V.&option=202" target="_blank" rel="nofollow">Alfimov Michael V.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Ya. Melnikov Mikhail&option=202" target="_blank" rel="nofollow">Ya. Melnikov Mikhail;</a> </p> <span class="z_kbtnclass z_kbtnclassall hoverxs" id="zkzz" style="display: none;">展开▼</span> </div> </li> <li> <div style="display: flex;"> <span class="lefttit">作者单位</span> <div style="position: relative;margin-left: 3px;max-width: 639px;"> <div class="threelineshidden zhankaihshouqi" id="fOrgthree"> <p>Chemistry DepartmentM. V. Lomonosov Moscow State UniversityMoscow Russian Federation;</p> <p>Chemistry DepartmentM. V. Lomonosov Moscow State UniversityMoscow Russian Federation;</p> <p>N. N. Semenov Institute of Chemical PhysicsRussian Academy of SciencesMoscow Russian Federation;</p> <p>N. N. Semenov Institute of Chemical PhysicsRussian Academy of SciencesMoscow Russian Federation;</p> <p>Chemistry DepartmentM. V. Lomonosov Moscow State UniversityMoscow Russian Federation;</p> <p>Photochemistry CenterRussian Academy of SciencesMoscow Russian Federation;</p> <p>Photochemistry CenterRussian Academy of SciencesMoscow Russian Federation;</p> <p>N. S. Kurnakov Institute of General and Inorganic ChemistryRussian Academy of SciencesMoscow Russian Federation;</p> <p>Chemistry DepartmentM. V. Lomonosov Moscow State UniversityMoscow Russian Federation;</p> <p>Photochemistry CenterRussian Academy of SciencesMoscow Russian Federation;</p> <p>Chemistry DepartmentM. V. Lomonosov Moscow State UniversityMoscow Russian Federation;</p> </div> <span class="z_kbtnclass z_kbtnclassall hoverxs" id="zhdw" style="display: none;">展开▼</span> </div> </div> </li> <li > <span class="lefttit">收录信息</span> <span style="width: 86%;vertical-align: text-top;display: inline-block;"></span> </li> <li> <span class="lefttit">原文格式</span> <span>PDF</span> </li> <li> <span class="lefttit">正文语种</span> <span>eng</span> </li> <li> <span class="lefttit">中图分类</span> <span><a href="https://www.zhangqiaokeyan.com/clc/4796.html" title="有机化学一般性问题">有机化学一般性问题;</a></span> </li> <li class="antistop"> <span class="lefttit">关键词</span> <p style="width: 86%;vertical-align: text-top;"> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=back electron transfer&option=203" rel="nofollow">back electron transfer;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=bis‐ammonium dipyridylethylene derivative&option=203" rel="nofollow">bis‐ammonium dipyridylethylene derivative;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=bis‐crown stilbene&option=203" rel="nofollow">bis‐crown stilbene;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=donor‐acceptor complex&option=203" rel="nofollow">donor‐acceptor complex;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=transient absorption&option=203" rel="nofollow">transient absorption;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=X‐ray diffraction&option=203" rel="nofollow">X‐ray diffraction;</a> </p> <div class="translation"> 机译:背电子转移;双氨二吡啶乙烯衍生物;双冠斯蒂尔贝烯;供体 - 受体复合物;瞬态吸收;X射线衍射; </div> </li> </ul> </div> </div> <div class="literature cardcommon"> <div class="similarity "> <h3 class="all_title" id="enpatent66">相似文献</h3> <div class="similaritytab clearfix"> <ul> <li class="active" >外文文献</li> <li >专利</li> </ul> </div> <div class="similarity_details"> <ul > <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/journal-foreign-detail/0704025793873.html">Complexation of bis‐crown stilbene with alkali and alkaline‐earth metal cations. 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style="display: none;"> <li> <div> <b>1. </b><a class="enjiyixqcontent" href="/patent-detail/06130471333561.html">METHOD OF ISOLATING WATER SOLUBLE CROWN-ESTERS CONTAINING 4 TO 6 ATOMS OF OXYGEN IN CYCLE FROM COMPLEXES WITH ALKALI OR ALKALINE-EARTH METALS</a> <b>[P]</b> . <span> 外国专利: <!-- --> SU1227632A1 </span> <span> . 1986-04-30</span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译:从含碱金属或碱土金属的配合物中分离出含4至6个原子的水溶性水溶性冠状酯的方法 </span> </p> </li> <li> <div> <b>2. </b><a class="enjiyixqcontent" href="/patent-detail/06130465964496.html">Reactions of bis-oxazolines with polycarboxylic acids catalyzed by alkali or alkaline earth metal cationic complexes</a> <b>[P]</b> . <span> 外国专利: <!-- 欧洲知识产权局专利: --> EP0216115B1 </span> <span> . 1990-07-11</span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译:碱或碱土金属阳离子配合物催化双恶唑啉与多元羧酸的反应 </span> </p> </li> <li> <div> <b>3. </b><a class="enjiyixqcontent" href="/patent-detail/06130467393173.html">REACTIONS OF BIS-OXAZOLINE WITH POLYCARBOXYLIC ACID CATALYZED BY ALKALI OR ALKALINE EARTH METAL CATIONIC COMPLEX</a> <b>[P]</b> . <span> 外国专利: <!-- --> CA1262297A </span> <span> . 1989-10-10</span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译:碱或碱土金属阳离子络合物催化的BIS-恶唑啉与多羧酸的反应 </span> </p> </li> </ul> </div> </div> </div> <div class="theme cardcommon" style="overflow: auto;display:none"> <h3 class="all_title" id="enpatent55">相关主题</h3> <ul id="subject"> </ul> </div> </div> </div> </div> <div class="right rightcon"> <div class="details_img cardcommon clearfix" style="margin-bottom: 10px;display:none;" > </div> </div> </div> <div id="thesis_get_original1" class="downloadBth" 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