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相关概念视频

Chemical Shift: Internal References and Solvent Effects01:17

Chemical Shift: Internal References and Solvent Effects

644
In an NMR sample, precise measurement of the absolute absorption frequencies of nuclei is difficult. A standard internal reference compound is added, and the frequency difference between the reference signal and sample signals is measured.
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
644
Electrospray Ionization (ESI) Mass Spectrometry01:12

Electrospray Ionization (ESI) Mass Spectrometry

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Higher molecular weight biomolecules are nonvolatile compounds that may decompose before ionizing or vaporizing during mass analysis with conventional electron impact ionization methods. Accordingly, electrospray ionization (ESI) is the favored method for vaporizing and ionizing biomolecules as it circumvents rapid fragmentation and enables the recording of mass signals for the entire biomolecule.
ESI utilizes electrical energy to transfer ions from the liquid phase of the sample into the...
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¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR01:15

¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR

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The axial and equatorial protons in cyclohexane can be distinguished by performing a variable-temperature NMR experiment. In this process, except for one proton, the remaining eleven protons are replaced by deuterium. The deuterium substitution avoids the possible peak splitting caused by the spin-spin coupling between the adjacent protons. The remaining proton flips between the axial and equatorial positions.
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¹H NMR Chemical Shift Equivalence: Homotopic and Heterotopic Protons01:03

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Protons in identical electronic environments within a molecule are chemically equivalent and have the same chemical shift. The replacement test is a useful tool to identify chemical equivalence and predict NMR spectra. A substituent replaces each of the protons being examined and the resulting molecules are compared. If the same molecule is obtained, the protons are equivalent or homotopic. Replacement of any hydrogens in ethane by chlorine yields chloroethane because all six protons are...
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相关实验视频

Updated: Jul 5, 2025

Preparation of Binary and Ternary Deep Eutectic Systems
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一种固态核磁共振方法用于制药用eutectic的特征.

Chaithanya Hareendran1,2, Parth S Shaligram2,3, Rajesh Gonnade2,3

  • 1Central NMR facility and Physical/Materials Chemistry Division, CSIR-National Chemical Laboratory, Pune 411008, India. tg.ajithkumar@ncl.res.in.

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这项研究表明,1H快速魔力角度旋转固态NMR可以通过检测分子间键来证实制药性性形成,这提供了一个超出微分扫描热量计的新分析方法.

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科学领域:

  • 制药科学 制药科学
  • 固态化学 固态化学
  • 分析化学 分析化学

背景情况:

  • 制药用品对药物配方开发至关重要.
  • 目前,差分扫描热度计 (DSC) 是确认体形成的主要方法.
  • 需要采用替代或补充技术来验证体结构.

研究的目的:

  • 为了证明1H快速神奇角度旋转 (MAS) 固态NMR (SSNMR) 的实用性,以证实药物体形成.
  • 通过使用SSNMR. 识别分子间结作为欧特克形成的关键指标.
  • 为DSC提供一种替代或补充的方法,用于Eutectic分析.

主要方法:

  • 使用了1H快速魔力角度旋转 (MAS) 固态NMR (SSNMR) 光谱.
  • 专注于检测在药物优质混合物中的分子间结相互作用.
  • 将SSNMR发现与DSC等传统方法进行了比较.

主要成果:

  • 通过使用1H MAS SSNMR.成功证实了制药性尤特克的形成.
  • 证明SSNMR可以直接检测出幼虫特有的分子间键.
  • 提供了证据表明SSNMR是一种可行的技术,用于分析eutectic系统.

结论:

  • 1H MAS SSNMR是一种强大的技术,用于确认制药品的体形成.
  • 通过SSNMR检测分子间的键,可以作为eutectic的可靠指标.
  • 这项研究扩大了制药配方科学家的分析工具包.