無液氦小型核磁共振波譜儀
核磁共振（NMR）技術本身可以實現(xiàn)物質(zhì)的結(jié)構(gòu)解析，通過測定樣品溶液的各譜圖，可以判斷其結(jié)構(gòu)。
應用：DNP-NMR,2D-NMR,多維核磁共振,動態(tài)核極化,混合物分析,組分分析,結(jié)構(gòu)分析
小型核磁共振波譜儀（NMR）特點：
◆ Elmathron® Patent 技術: 低場DNP-NMR
( US 10, 773, 092 B2）
◆ 澆筑型聚焦式永磁鐵設計
◆ 超計算能力 ，進行物質(zhì)結(jié)構(gòu)分析
◆ 強大的數(shù)據(jù)庫，可實時顯示所含混合物, 物質(zhì)種類及含量
◆ 靈敏度高，液體或氣體檢測需量少
◆ 可提供原始數(shù)據(jù)，用于客戶自行建模
◆ 應用軟件界面友好，功能強大，使用方便
低成本，無需液氦制冷，免維護型實時NMR設備！
重量：18 kg
體積：50cm×30cm×15cm
FAQ:
Q: What is the magnetic strength in Tesla?
A: We use very weak magnets, only 1 T, because DNP in liquids only works well with magnetic fields less than 1 T. In turn, DNP improves the signal-to-noise ratio for one-dimensional spectra by about 400 times, and almost 100,000 times for multidimensional spectra. Therefore, the sensitivity of 1D is approximately as if we were capturing spectra at 100 MHz, and the sensitivity of 2D+ is approximately as if we were capturing spectra at 400 MHz.
Q: Can I get 1D spectra from Elegant NMR system?
A: The ability of the Elegant NMR measuring system to automatically interpret heteronuclear DNP NMR spectra on an adaptive grid completely disrupts the status quo in which 7- and 8- dimensional DNP NMR spectra, having sparsity values less than 0.1%, are very difficult not only to interpret, but even to visualize.
In the Elegant NMR system, such spectra are identified with reference to a huge database con-taining about 1.7 billion spatial molecular structures.
7-8-dimensional spectra can be projected onto one-dimensional slices and then visualized. We will implement this approach in the expert mode of the Elegant NMR software for reference purposes.
Q: Do we need to use external MW source for DNP?
A: No, Elegant NMR System is equipped with internal DNP source according to recently patented technology US B2.
Q: Do you have HPLC/GCMS inside, or how you separate unknown mixtures?
A: We do not separate molecules, we separate signals. In classical HPLC, for separation to occur, we need the substances to be separated to form complexes with a stationary phase and the energy of formation of such complexes is significantly different. It is often possible to find a stationary phase that would orientate the substances to be separated well, but would not separate these mixtures well enough, for instance, because of the insufficient number of theoretical plates. In our apparatus we do not separate substances, namely, we orient them differently. This orientation affects the two-dimensional NMR spectra and it is possible, without separation, to obtain slightly different HSQC or NOE spectra, and on the basis of their correlations, to get relative concentration and pure spectra of the substances themselves.
