• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

Low-temperature spectral observation of the first six-coordinate nitrosyl complexes of cobalt(II) meso-tetratolylporphyrin with trans nitrogen base ligands.

作者信息

Kurtikyan Tigran S, Markaryan Emil R, Mardyukov Artur N, Goodwin John A

机构信息

Molecule Structure Research Center NAS, 26 Azatutyan av, 375014 Yerevan, Armenia.

出版信息

Inorg Chem. 2007 Mar 5;46(5):1526-8. doi: 10.1021/ic062070y. Epub 2007 Feb 7.

DOI:10.1021/ic062070y
PMID:17284028
Abstract

Low-temperature interaction of nitrogen base ligands with layered Co(TTP)(NO) (TTP = meso-tetratolylporphyrinato dianion) as well as its toluene solution leads to the formation of the first six-coordinate species of the general formula (B)Co(TTP)(NO) (where B = piperidine and pyridine). The nu(NO) stretching bands of these species appear at lower frequencies compared with the five-coordinate nitrosyl derivative and depend on the nature of the trans axial ligand. The equilibrium constants and enthalpies of formation of these new species are determined. Fairly stable at low-temperature conditions in the solid state, they slowly dissociate the nitrogen base ligands upon warming to restore the five-coordinate nitrosyl complex Co(TTP)(NO).

摘要

相似文献

1
Low-temperature spectral observation of the first six-coordinate nitrosyl complexes of cobalt(II) meso-tetratolylporphyrin with trans nitrogen base ligands.
Inorg Chem. 2007 Mar 5;46(5):1526-8. doi: 10.1021/ic062070y. Epub 2007 Feb 7.
2
Six-coordinate nitrosyl and nitro complexes of meso-tetratolylporphyrinatocobalt with trans sulfur-donor ligands.六配位亚硝酰和硝基配合物meso-四甲苯基卟啉钴与反式硫给体配体。
Inorg Chem. 2010 Sep 6;49(17):7793-8. doi: 10.1021/ic1007846.
3
Reactions of nitrogen oxides with the five-coordinate Fe(III)(porphyrin) nitrito intermediate Fe(Por)(ONO) in sublimed solids.氮氧化物与升华固体中五配位铁(III)(卟啉)亚硝酸根中间体Fe(Por)(ONO)的反应。
J Am Chem Soc. 2007 Mar 28;129(12):3576-85. doi: 10.1021/ja067245h. Epub 2007 Mar 6.
4
Six-coordinate nitrato complexes of iron(III) porphyrins.铁(III)卟啉的六配位硝酸根配合物。
Inorg Chem. 2008 Feb 4;47(3):787-9. doi: 10.1021/ic702102j. Epub 2007 Dec 29.
5
Reactions of NO with Mn(II) and Mn(III) centers coordinated to carboxamido nitrogen: synthesis of a manganese nitrosyl with photolabile NO.一氧化氮与配位在羧酰胺氮上的锰(II)和锰(III)中心的反应:一种具有光不稳定一氧化氮的亚硝酰锰的合成。
Inorg Chem. 2004 May 3;43(9):2988-97. doi: 10.1021/ic030331n.
6
Weak coordination of neutral S- and O-donor proximal ligands to a ferrous porphyrin nitrosyl. Characterization of 6-coordinate complexes at low T.弱配位中性 S 和 O 供体近端配体与亚铁卟啉亚硝酰基。低温下 6 配位配合物的特性。
J Inorg Biochem. 2013 Apr;121:129-33. doi: 10.1016/j.jinorgbio.2012.12.017. Epub 2013 Jan 10.
7
Nitric oxide dioxygenation reaction by oxy-coboglobin models: in-situ low-temperature FTIR characterization of coordinated peroxynitrite.氧合肌红蛋白模型的一氧化氮双氧反应:配位过氧亚硝酸盐的原位低温 FTIR 表征。
J Am Chem Soc. 2012 Aug 22;134(33):13861-70. doi: 10.1021/ja305774v. Epub 2012 Aug 10.
8
Nitric oxide interaction with oxy-coboglobin models containing trans-pyridine ligand: two reaction pathways.一氧化氮与含反式吡啶配体的氧合钴血红蛋白模型的相互作用:两条反应途径。
Inorg Chem. 2013 Oct 21;52(20):12046-56. doi: 10.1021/ic4018689. Epub 2013 Oct 3.
9
Ruthenium nitrosyls derived from polypyridine ligands with carboxamide or imine nitrogen donor(s): isoelectronic complexes with different NO photolability.源自具有甲酰胺或亚胺氮供体的多吡啶配体的亚硝酰钌:具有不同NO光解性的等电子配合物
Inorg Chem. 2007 Mar 19;46(6):2328-38. doi: 10.1021/ic0620945. Epub 2007 Feb 22.
10
Iron-porphyrin NO complexes with covalently attached N-donor ligands: formation of a stable six-coordinate species in solution.铁卟啉-NO 配合物与共价键合的 N-供体配体:溶液中稳定的六配位物种的形成。
J Am Chem Soc. 2009 Dec 2;131(47):17116-26. doi: 10.1021/ja904368n.