N-[4-(bromomethyl)phenyl]methyl-N'-[4-(trimethoxysilyl)phenyl]methyl-4,4'-bipyridinium | 112818-38-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: N-[4-(bromomethyl)phenyl]methyl-N'-[4-(trimethoxysilyl)phenyl]methyl-4,4'-bipyridinium
• CAS: 112818-38-9
• 化学式: C₂₈H₃₁BrN₂O₃Si
• 分子量: 551.555
• InChiKey: POPBBZRSWPMVMO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.01
• 重原子数：
  35.0
• 可旋转键数：
  10.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  35.45
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  2,5-dichloro-3,6-bis<(2-(dimethylamino)ethyl)-amino>-1,4-benzoquinone 、 N-[4-(bromomethyl)phenyl]methyl-N'-[4-(trimethoxysilyl)phenyl]methyl-4,4'-bipyridinium 以 二甲基亚砜 为溶剂， 反应 3.0h， 生成 1',1'''-(((((((2,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,4-diyl)bis(azanediyl))bis(ethane-2,1-diyl))bis(dimethylammoniumdiyl))bis(methylene))bis(4,1-phenylene))bis(methylene))bis(1-(4-(trimethoxysilyl)benzyl)-[4,4'-bipyridine]-1,1'-diium)
  参考文献：
  名称：

  电极约束的氧化还原聚合物的电荷传输性质，该聚合物由包含两个苄基紫罗兰亚基侧翼的醌组成的单体组成

  摘要：

  DOI：

  10.1021/j100320a044
• 作为产物：
  描述：

  4,4'-联吡啶 以 乙腈 为溶剂， 反应 5.0h， 生成 N-[4-(bromomethyl)phenyl]methyl-N'-[4-(trimethoxysilyl)phenyl]methyl-4,4'-bipyridinium
  参考文献：
  名称：

  电极约束的氧化还原聚合物的电荷传输性质，该聚合物由包含两个苄基紫罗兰亚基侧翼的醌组成的单体组成

  摘要：

  DOI：

  10.1021/j100320a044

文献信息

• pH-Dependent Rectification in Redox Polymers:  Characterization of Electrode-Confined Siloxane Polymers Containing Naphthoquinone and Benzylviologen Subunits
  作者：G. Tayhas R. Palmore、Diane K. Smith、Mark S. Wrighton

  DOI：10.1021/jp9626475

  日期：1997.4.1

  This paper describes the electrochemical characterization of electrode-confined siloxane polymers that contain both naphthoquinone (NQ) and benzylviologen (BV2+) subunits. These ''homopolymers,'' abbreviated (NQ-BV3+)(n) and (NQ-BV-BV5+)(n), are derived from monomers, 2-chloro-3-[[2-dimethyl[[[[N'-[[4-(trimethoxysilyl)- phenyl]methyl]-4,4'-bipyridiniumyl]methyl]phenyl]methyl]ammonium}ethyl]amino]-1,4-naphthoquinone, 1a, and 2-chloro-3-[[2-dimethyl[[[[[[[[N'-[N'-[[4-(trimethoxysilyl)phenyl]methyl]-4,4'bipyridiniumyl]methyl]- phenyl]methyl]-4,4'-bipyridiniumyl]methyl]phenyl]methyl]ammonium}ethyl]amino]-1,4-naphthoquinone, 2a, respectively. Particular to these types of surface-confined homopolymers is the ability to ''trap'' charge at low pH in the form of reduced quinone. Between pH 10.0 and 7.0, (NQ-BV3+)(n) and (NQ-BV-BV5+)(n) undergo reversible 3e-/2H(+) and 4e-/2H(+) reduction, respectively, consistent with 2e-/2H(+) reduction of NQ subunits to the hydroquinone NQH(2) and 1e- reduction of BV2+ subunits to the radical cation BV+.. Below pH 6, however, NQ/NQH(2) reduction becomes irreversible in both polymers, whereas BV2+/+ reduction remains reversible. Electrochemical irreversibility of NQ/NQH(2) in these polymers occurs because its electrochemistry is mediated by the BV2+/+ couple. Between pH 10.0 and 7.0, BV2+/+ can mediate both reduction and oxidation of NQ/NQH(2), whereas below pH 6, the thermodynamics are such that BV2+/+ can only mediate the reduction of NQ. This behavior is similar to that of a previously studied (benzylviologen)-benzoquinone-(benzylviologen) polymer, (BV-Q-BV6+)(n).(1) Charge in the form of reduced quinone is trapped in (BV-Q-BV6+)(n) at low pH because there is essentially no direct charge transport through the Q/QH(2) system. Charge is also trapped in high coverages of (NQ-BV3+)(n) and (NQ-BV-BV5+)(n), indicating no direct charge transport through the NQ/NQH(2) system. Unlike (BV-Q-BV6+)(n), however, monolayers comprised of 1a or 2a exhibit charge transport through the NQ/NQH(2) system. The flexibility of these monolayers apparently allows direct contact of the NQ subunit with the electrode surface. Less flexible and more robust surface-confined polymers, abbreviated (NQ-BV3+/siloxane)(n) and (NQ-BV-BV5+/siloxane)(n), can be prepared by copolymerization of 1a or 2a with 1,2-bis(trimethoxysilyl)ethane. Charge trapped in (NQH(2)-BV3+/siloxane)(n) or (NQH(2)-BV-BV5+/siloxane)(n) can be released and delivered to the surface of the electrode via chemical mediation or by an increase in solution pH. For example, the redox couple I-3(-)/I- will catalytically release the trapped charge when the potential of the electrode is brought close to E(o)'(I-3(-)/I-). Surfaces modified with (NQ-BV3+/siloxane)(n) or (NQ-BV-BV5+/siloxane)(n), however, are impermeable to the large anionic redox couple Fe(CN)(6)(3-/4-), preventing mediated charge release by this reagent.The lack of electrostatic binding of Fe(CN)(6)(3-/4-) to electrodes modified with (NQ-BV3+/siloxane)(n) or (NQ-BV-BV5+/siloxane)(n) suggests a high degree of crosslinking in these polymers provided by 1,2-bis(trimethoxysilyl)ethane. At neutral pH, dioxygen will chemically induce the release of charge trapped in (NQH(2)-BV3+/siloxane)(n) or (NQH(2)-BV-BV5+/siloxane)(n). The irreversible production of H2O2 upon oxidation of NQH(2) in water, however, prevents the return of charge to the electrode. Charge release is also demonstrated by pH jump experiments where an increase in pH shifts E(o)'(NQ/NQH(2)) to a potential where BV2+/+ mediate the oxidation of NQH(2) to NQ and deliver charge to the electrode.