1H T1ρ based ROSY: NMR spectral fingerprints for nanoscale phase separated structure of block copolymers

被引:3
作者
Yazawa, Koji [1 ]
Asakawa, Naoki [2 ,3 ]
Nishiyama, Yusuke [1 ,4 ]
机构
[1] JEOL RESONANCE Inc, Akishima, Tokyo 1968558, Japan
[2] Gunma Univ, Grad Sch Sci & Technol, 1-5-1 Tenjin Cho, Kiryu, Gumma 3768515, Japan
[3] Gunma Univ, Ctr Food Sci & Wellness, 1-5-1 Tenjin Cho, Kiryu, Gumma 3768515, Japan
[4] RIKEN, Nanocrystallog Unit, RIKEN JEOL Collaborat Ctr, Yokohama, Kanagawa 2300045, Japan
关键词
Block copolymer; Nanoscale phase separation; Spectral fingerprint; Solid-state NMR; Spin diffusion; ROSY; T-1; rho; DOMAIN SIZES; TEMPERATURE; POLYMERS; MISCIBILITY; THERMOMETER; RELAXATION; MORPHOLOGY; BLENDS; FILMS;
D O I
10.1007/s11696-022-02441-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A nuclear magnetic resonance (NMR) fingerprinting method for nanoscale phase-separated block copolymers (BCPs) consisting of hard and soft segments is introduced. The separation of C-13 spectra is performed using H-1 longitudinal relaxation time in rotating frame (T-1 rho(H))-based ROSY (Relaxation Ordered SpectroscopY) method which uses an inverse Laplace transform of the relaxation time dimension. The method was first validated on a model sample, poly(3-hexylthiophene) (P3HT), as a well-characterized system analogous to phase-separated BCP consisting of soft and hard segments. Then, the method was applied to a class of BCPs, polyurethane. The basic set of solid-state NMR experiments, C-13 direct-polarization magic angle spinning (MAS) obtained with short recycling delays and cross-polarization MAS, which provide C-13 NMR spectra of the mobile and rigid components, respectively, often fail to separate the C-13 NMR spectra of soft and hard segments of BCP. On the other hand, the ROSY separates the C-13 NMR spectra of BCP consisting of nanophase-separated soft and hard segments into their respective segments. This method is useful not only for structure determination of hard and soft domains but also as spectral fingerprinting. [GRAPHICS] .
引用
收藏
页码:7783 / 7792
页数:10
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