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Nitroxide radicals for low frequency electron paramagnetic resonance imaging (EPRI).

机译:用于低频电子顺磁共振成像(EPRI)的一氧化氮自由基。

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摘要

Optimization of nitroxides as probes for EPR imaging requires detailed understanding of spectral properties such as spin lattice relaxation times, spin packet linewidths, and nuclear hyperfine splitting. Initial measurements of relaxation times for six low molecular weight nitroxides at X-band stimulated further measurement at frequencies between 250 MHz and 34 GHz. The impact of tumbling was studied with perdeuterated 2,2,6,6-tetramethyl-4-piperidinyl-1-oxyl (PDT) in five solvents with viscosities resulting in tumbling correlation times, tauR, between 4 and 50 ps. A set of three 14N/ 15N pairs of nitroxides in water was selected such that tau R varied between 9 and 19 ps. To test the impact of structure on relaxation, three additional nitroxides with tauR between 10 and 26 ps were studied.;In the fast tumbling regime 1/T2 ∼ 1/T1 and relaxation is dominated by spin rotation, modulation of A-anisotropy and a thermally activated process. The contribution to 1/T1 from spin rotation is independent of frequency and decreases as tauR increases. The modulation of nitrogen hyperfine anisotropy increases as frequency decreases and as tauR increases, dominating at low frequencies for tau R∼ 15 ps. The modulation of g anisotropy is significant only at 34 GHz. Inclusion of a thermally activated process was required to account for the observation that for most of the radicals, 1/T1 was smaller at 250 MHz than at 1-2 GHz. The thermally activated process likely arises from intramolecular motions of the nitroxide ring that modulate the isotropic A values.;A phantom of three 4 mm tubes containing different 15N, 2H-substituted nitroxides was constructed for use at 250 MHz. Projections for 2D spectral-spatial images were obtained by continuous wave (CW) and rapid scan (RS) EPR using a bimodal cross-loop resonator. Relative to CW projections obtained for the same data acquisition time (5 min), RS projections had significantly improved image quality. All experiments were facilitated by advancements in resonator design and testing, which are also described.
机译:优化氮氧化物作为EPR成像的探针需要详细了解光谱特性,例如自旋晶格弛豫时间,自旋包线宽和核超细分裂。在X波段对六种低分子量氮氧化物的弛豫时间进行初步测量,激发了在250 MHz至34 GHz之间的频率下进行进一步测量。在5种溶剂中使用全氘化的2,2,6,6-四甲基-4-哌啶基-1-氧基(PDT)研究了翻滚的影响,其粘度导致翻滚相关时间tauR在4到50 ps之间。选择一组水中的三对14N / 15N氮氧化物,以使tau R在9 ps至19 ps之间变化。为了测试结构对弛豫的影响,研究了另外三个tauR在10到26 ps之间的一氧化氮。在快速翻转状态1 / T2〜1 / T1中,弛豫主要由自旋旋转,A各向异性的调制和a热活化过程。自旋旋转对1 / T1的贡献与频率无关,并且随着tauR的增加而减小。氮的超细各向异性的调制随着频率的降低和tauR的增加而增加,在tau R〜15 ps的低频下占主导地位。 g各向异性的调制仅在34 GHz时才有意义。对于大多数自由基,在250 MHz时,1 / T1小于在1-2 GHz时的观测值,因此需要包括热活化过程。热活化过程可能是由调节各向同性A值的氮氧化物环的分子内运动引起的。构造了三个4毫米管的幻像,其中包含不同的15N,2H取代的氮氧化物,用于250 MHz。使用双峰交叉回路谐振器通过连续波(CW)和快速扫描(RS)EPR获得2D光谱空间图像的投影。相对于相同的数据采集时间(5分钟)获得的CW投影,RS投影显着改善了图像质量。谐振器设计和测试的进步也促进了所有实验的进行,并对此进行了描述。

著录项

  • 作者

    Biller, Joshua R.;

  • 作者单位

    University of Denver.;

  • 授予单位 University of Denver.;
  • 学科 Chemistry Biochemistry.;Chemistry Physical.;Chemistry Organic.;Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 279 p.
  • 总页数 279
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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