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Mnemonic Device for the Spin-Spin Spiitting for Three Protons.

Mnemonic for determining if a iigand is a one-electron or two-electron donor.

Mnemonic for determining the order of filling of orbitals . Adapted from Moeller, T. Inorganic Chemistry Wiley

Mnemonic for DPPBA-based ligand in the ionization.

Mnemonic for electronic configuration determination based on the Aufbau principle.

Mnemonic for prediction of stereoselection in Deng s ASD of achiral meso-anhydrides .

Mnemonic for remembering the 10 essential amino acids .

Mnemonic to obtain the order of filling of orbitals.

Mnemonic Tor determining the order or filling of orbitals . Adapted from Moeller, T. Inorganic Chemistry Wiley

MNEXD heats of formation for normal valence isomers within the ensembles C4H3S and C4H3O , 1

MnfCHjCOOlj 4H2O, single crystal. Resonance diagram for H parallel to the c axis and T 1.2K. Solid line, theoretical curve circles, experimental data dotted line, best fit ,

MnIV3 . Reproduced with permission from

Mnj 2thf. Temperature dependence of 1 Xm- Curve 1 fitted according to radical ion model using 2 k -200K, g 2.00. Curve 2 represents susceptibility fitted according to radical ion model corrected for 6 -4K J k -200K, g 2.0. For details see original literature .

Mnj04 . Temperature dependence of l x .

MnjB4 single crystal. Temperature dependence of Zg .

MnjCl2. Temperature dependence of Curves fitted according to anti-ferromagnetic Heisenberg linear-chain model full curve

MnjLaj,2 -24H20, single crystal. Temperature dependence of principal susceptibilities, divided by the Curie constant C below 1 K.

MnjLaji2 24H2O, single crystal. Isentropes in the H-T diagram. The magnetic field was directed along the c axis .

MnjP207, single crystal. Susceptibility at 4.2 K in a-b plane .

MnjPjO, single crystal. Temperature dependence of for the applied field H in two directions in a-c plane .

MnjSij . Temperature dependence of Xe .

Mnk cular Mrucluiv ol EiMg,Cli-, illuMraiiiig scleclcd bond distances and angles 15.5.

MNK rearrangement for the production of sUyl thiocarbamates and the resulting yields

MNK rearrangement for the synthesis of substituted benzothiophenes

MNK rearrangement in a -helicene



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