Suppr超能文献

中性有机金属卤素键受体:PCPPdX(X = Cl、Br、I)与碘(I₂)、1,4 - 二碘四氟苯(F₄DIBz)和1,4 - 二碘八氟丁烷(F₈DIBu)形成的配合物中的卤素键

Neutral Organometallic Halogen Bond Acceptors: Halogen Bonding in Complexes of PCPPdX (X = Cl, Br, I) with Iodine (I(2)), 1,4-Diiodotetrafluorobenzene (F4DIBz), and 1,4-Diiodooctafluorobutane (F8DIBu).

作者信息

Johnson Magnus T, Džolić Zoran, Cetina Mario, Wendt Ola F, Ohrström Lars, Rissanen Kari

出版信息

Cryst Growth Des. 2012 Jan 1;12(1):362-368. doi: 10.1021/cg201170w. Epub 2011 Nov 17.

Abstract

The behavior of a sterically crowded neutral pincer {2,6-bis[(di-t-butylphosphino)methyl]-phenyl}palladium (PCPPd) halides, PCPPdX (X = Cl, Br or I), as XB acceptors with strong halogen bond (XB) donors, iodine (I(2)), 1,4-diiodotetrafluorobenzene (F4DIBz), and 1,4-diiodooctafluorobutane (F8DIBu) were studied in the solid state. The co-crystallization experiments afforded high-quality single crystals of XB complexes PCPPdCl-I(2) (1a), PCPPdBr-I(2) (2a), PCPPdI-I(2)(3a), PCPPdCl-F4DIBz (1b), PCPPdBr-F4DIBz (2b), and PCPPdBr-F8DIBu (2c). The 1:1 iodine complexes (1a, 2a, and 3a) all showed a strong halogen bonding interaction, the reduction of the sum of the van der Waals radii of halogen to iodine being 24.6 (1a), 23.9 (2a), and 19.4% (3a) with X···I-I angles of 177, 176, and 179°, respectively. While the pincer palladium chloride 1 and bromide 2 were crystallographically isomorphous and showed similar XB behavior, the palladium iodide complex, 3, exhibited markedly different properties, and unlike 1 and 2 it does not, under similar conditions, result in XB complexes with the weaker XB donors F4DIBz and F8DIBu. The results indicate that PCPPdI is not nucleophilic enough to have XB interactions with other donors than iodine. However, the weaker XB donors F4DIBz and F8DIBu form XB complexes with the chloride 1 and especially with the bromide 2. The prevalence of the halogen bonding with 2 is probably not only electronic in origin, and it seems to offer the best balance between electron poorness and steric availability. The XB interactions with F4DIBz and F8DIBu are much weaker than with iodine, the reduction of the sum of the van der Waals radii of halogen to iodine being 13.5, 12.3, and 14.6% with C-I···X angles between 163 and 179° for 1b, 2b, and 2c, respectively, and results in polymeric (···1···F4DIBz···1···F4DIBz···)(n), (···2···F4DIBz···2···F4DIBz···)(n), and (···2···F8DIBu···2···F8DIBu···)(n) one-dimensional zigzag chains in the solid state.

摘要

研究了空间位阻较大的中性钳形化合物{2,6-双[(二叔丁基膦基)甲基]-苯基}钯(PCPPd)卤化物PCPPdX(X = Cl、Br或I)作为卤键(XB)受体与强卤键供体碘(I₂)、1,4-二碘四氟苯(F₄DIBz)和1,4-二碘八氟丁烷(F₈DIBu)在固态下的行为。共结晶实验得到了卤键配合物PCPPdCl-I₂ (1a)、PCPPdBr-I₂ (2a)、PCPPdI-I₂(3a)、PCPPdCl-F₄DIBz (1b)、PCPPdBr-F₄DIBz (2b)和PCPPdBr-F₈DIBu (2c)的高质量单晶。1:1碘配合物(1a、2a和3a)均显示出强烈的卤键相互作用,卤原子与碘的范德华半径之和的减小率分别为24.6% (1a)、23.9% (2a)和19.4% (3a),X···I-I角度分别为177°、176°和179°。虽然钳形钯氯化物1和溴化物2在晶体结构上是同构的,并且表现出相似的XB行为,但碘化钯配合物3表现出明显不同的性质,与1和2不同,在相似条件下,它不会与较弱的XB供体F₄DIBz和F₈DIBu形成XB配合物。结果表明,PCPPdI的亲核性不足以与除碘以外的其他供体发生XB相互作用。然而,较弱的XB供体F₄DIBz和F₈DIBu与氯化物1,特别是与溴化物2形成XB配合物。与2形成卤键的普遍性可能不仅源于电子因素,而且似乎在电子贫化和空间可及性之间提供了最佳平衡。与F₄DIBz和F₈DIBu的XB相互作用比与碘的相互作用弱得多,卤原子与碘的范德华半径之和的减小率分别为13.5%、12.3%和14.6%,1b、2b和2c的C-I···X角度在163°至179°之间,并且在固态下形成聚合物(···1···F₄DIBz···1···F₄DIBz···)ₙ、(···2···F₄DIBz···2···F₄DIBz···)ₙ和(···2···F₈DIBu···2···F₈DIBu···)ₙ一维锯齿链。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fac2/3252960/c20e13caa375/cg-2011-01170w_0005.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验