Dinitroxide-type biradical compounds optimized for dynamic nuclear polarization (DNP)
The present invention relates to the field of organic chemistry and in particular to organic free radicals used as polarizing agents in the technique of Dynamic Nuclear Polarization (DNP), which involves transferring the polarization of electron spins to the nuclei of a compound whose Nuclear Magnetic Resonance (NMR) is being observed. It concerns dinitroxide-type biradical polarizing agents characterized by a rigid linkage between the nitroxide units that enables optimal orientation and distance to be maintained between the aminoxyl groups of said nitroxide units. This particular structure enables, at low temperatures and high fields, optimal transfer of polarization and optimal enhancement of NMR/MAS signals of the polarized nuclei of the compound studied.
1. A dinitroxide-type biradical compound comprising:
a rigid linkage between the two nitroxide units that maintains a specific orientation and distance between the two aminoxyl groups of these units, said rigid linkage being an odd number of spiranic bonds, wherein the dinitroxide-type biradical compounds are of the general formula:
in which X is a single bond between the atoms n−1 and n+1, or O, N, N(O), S, S(O), SO2, or a (C1-C4) alkyl chain,
in which Y1 is a single bond between the atoms n−1 and n+1, or O, N, N(O), S, S(O), SO2, or a (C1-C4) alkyl chain,
in which Y2 is a single bond between the atoms n−1 and n+1, or O, N, N(O), S, S(O), SO2, or a (C1-C4) alkyl chain,
in which Z1=—R1 or —R1-R2 and Z2=—R1 or —R1-R2, where R1 is selected from the group consisting of a chain of (C1-C17) alkyl, cycloalkyl, heterocycloalkyl, spirocycloalkyl, spiroheterocycloalkyl, alkenyl, alkynyl, (C6-C18) aryl, and R2 is selected from the group consisting of H, hydroxyl (—OH), primary amine (—NH2), secondary amine (—NH), tertiary amine (—N), ammonio (—N + ), amine oxide (—NO), carboxyl (—COOH), sulfanyl (—SH), polyethylene-glycol (CH2-CH2-O)n-CH2X, X being OH or NH2), sulfinyl (—SO), sulfonyl (—SO2), sulfonato (—SO 3 − ), phosphono (—PO3H2, —PO3R2 where R is (C1-C17) alkyl or (C6-C18) aryl), phosphoryl (—P(O)R2 where R—(C1-C17) alkyl, (C6-C18) aryl), phosphonio (—P + ), phosphoric ester (—O—PO 3 − ), wherein
the dinitroxide-type biradical compounds further include the addition of at least one chemical group that facilitates solubility, selected from among the functions and groups of hydroxyl (—OH), primary amine (—NH2), secondary amine (—NH), tertiary amine (—N), ammonio (—N + ), amine oxide (—NO), carboxyl (—COOH), sulfonyl (—SH), polyethylene-glycol (CH2-CH2-O)n-CH2X, where X is OH or NH2) sulfinyl (—SO), sulfonyl (—SO2), sulfonato (—SO 3 − ), phosphono (—PO3H2, —PO3R2 where R is (C1-C17) alkyl or (C6-C18) aryl), phosphoryl (—P(O)R2 where R is (C1-C17) alkyl or (C6-C18) aryl), phosphonio (—P + ), phosphoric ester (—O—PO 3 − ).
2. The dinitroxide-type biradical compound of claim 1 , in which the linkage between the two nitroxide units enables a stable conformation to be obtained in which the nodal plans of the aminoxyl groups of these two units create between them an angle between 65° and 115°, inclusive.
3. The dinitroxide-type biradical compound of claim 1 , in which the linkage between the two nitroxide units enables the nitrogen atoms of the aminoxyl groups of the nitroxide units to be maintained at a distance of between 3 and 16 A.
4. The dinitroxide-type biradical compound of claim 1 , in which the nitroxide units are selected from units of piperidinoxyl, pyrrolidinoxyl, imidazolinoxyl, imidazolidinoxyl, oxazolidinoxyl and nitronylnitroxide.
5. The dinitroxide-type biradical compound of claim 1 , characterized by the addition of at least one photosensitizing group selected from thioxanthone, benzoin, benzyl dimethyl acetal or benzophenone.
6. The dinitroxide-type biradical compound of claim 1 , characterized by the addition of at least one chemical group reactive with respect to the groups —SH, —NH2, —NH—, —OH, —COOH, hydroxyaryl (ArOH) such as:
7. The dinitroxide-type biradical compound of claim 1 , characterized by their conjugation to biomolecules selected from proteins, ribosomes, lipids, saccharides, DNA, RNA.
8. The dinitroxide-type biradical compound of claim 1 , which are isotopically labeled with an atom selected from Deuterium ( 2 H), Carbon 13 ( 13 C) and Nitrogen 15 ( 15 N).
9. A dinitroxide-type biradical compound comprising:
a rigid linkage between the two nitroxide units that maintains a specific orientation and distance between the two aminoxyl groups of these units, said rigid linkage being an odd number of spiranic bonds, wherein the dinitroxide-type biradical compounds are of the general formula:
in which X is a single bond between the atoms n−1 and n+1, or O, N, N(O), S, S(O), SO2, or a (C1-C4) alkyl chain,
in which Y1 is a single bond between the atoms n−1 and n+1, or O, N, N(O), S, S(O), SO2, or a (C1-C4) alkyl chain,
in which Y2 is a single bond between the atoms n−1 and n+1, or O, N, N(O), S, S(O), SO2, or a (C1-C4) alkyl chain,
in which Z 1 and Z 2 form together a (C4-C17) spirocycloalkyl or spiroheterocycloalkyl.
10. The dinitroxide-type biradical compound of claim 9 , further including the addition of at least one photosensitizing group selected from thioxanthone, benzoin, benzyl dimethyl acetal or benzophenone.
11. The dinitroxide-type biradical compound of claim 9 , which are isotopically labeled with an atom selected from Deuterium ( 2 H), Carbon 13 ( 13 C) and Nitrogen 15 ( 15 N).
12. The dinitroxide-type biradical compound of claim 1 , further including the addition of at least one photosensitizing group selected from thioxanthone, benzoin, benzyl dimethyl acetal or benzophenone.
13. The dinitroxide-type biradical compound of claim 1 , which are isotopically labeled with an atom selected from Deuterium ( 2 H), Carbon 13 ( 13 C) and Nitrogen 15 ( 15 N).