Magnetic Properties of Free Radicals · Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 1

Table of contents (61 documents)

1. Online Document 1

   I General introduction

   H. Fischer

2. Online Document 2

   III General symbols and abbreviations

   H. Fischer

3. Online Document 3

   13.1 Introduction

   S.R.A. Marque, P. Tordo

4. Online Document 4

   13.2 Phosphinyl radicals X2P• and related species

   S.R.A. Marque, P. Tordo

5. Online Document 5

   13.3 Phosphonyl (X2P•=O) and thiophosphonyl (X2P•=S) radicals

   S.R.A. Marque, P. Tordo

6. Online Document 6

   13.4 Phosphoranyl radicals X4P•, including related species

   S.R.A. Marque, P. Tordo

7. Online Document 7

   13.5 Phosphoniumyl cation radicals X3P•+, phosphine dimer cation radicals X3P•P+X3, phosphate anion radicals, and related species

   S.R.A. Marque, P. Tordo

8. Online Document 8

   13.6 Miscellaneous

   S.R.A. Marque, P. Tordo

9. Online Document 9

   14 Radicals centered on other heteroatoms

   R.F.C. Claridge

10. Online Document 10

    14.2.1 Thiyl radicals of the type RS•, R-S•R, R-S•-R2

    R.F.C. Claridge

11. Online Document 11

    14.2.2 Sulfinyl radicals of the type R-S•=O

    R.F.C. Claridge

12. Online Document 12

    14.2.3 Sulfonyl radicals of the type RS•O2

    R.F.C. Claridge

13. Online Document 13

    14.2.4 Sulfuranyl radicals of the type X-S•-R2, X2–S•-R, S•X3, S•X4

    R.F.C. Claridge

14. Online Document 14

    14.2.5 Disulfide radicals of the type R-S-S•

    R.F.C. Claridge

15. Online Document 15

    14.2.6 Cation radicals

    R.F.C. Claridge

16. Online Document 16

    14.2.7 Anion radicals

    R.F.C. Claridge

17. Online Document 17

    14.3.1 Silyl radicals X3Si•

    R.F.C. Claridge

18. Online Document 18

    14.3.2 Silyl radicals from polysilanes

    R.F.C. Claridge

19. Online Document 19

    14.3.3 Silicon-centered anion radicals

    R.F.C. Claridge

20. Online Document 20

    14.3.4 Silicon-centered anion radicals from polysilanes

    R.F.C. Claridge

21. Online Document 21

    14.3.5 Silicon-centered cation radicals

    R.F.C. Claridge

22. Online Document 22

    14.4.1 Germyl radicals X3Ge•

    R.F.C. Claridge

23. Online Document 23

    14.4.2 Germanium-centered anion radicals

    R.F.C. Claridge

24. Online Document 24

    14.4.3 Germanium-centered cation radicals

    R.F.C. Claridge

25. Online Document 25

    14.5.1 Stannyl radicals X3Sn•

    R.F.C. Claridge

26. Online Document 26

    14.5.2 Tin-centered anion radicals

    R.F.C. Claridge

27. Online Document 27

    14.5.3 Tin-centered cation radicals

    R.F.C. Claridge

28. Online Document 28

    14.6.1 Boryl radicals X3B•

    R.F.C. Claridge

29. Online Document 29

    14.6.2 Boron-centered anion radicals

    R.F.C. Claridge

30. Online Document 30

    14.6.3 Boron-centered cation radicals

    R.F.C. Claridge

31. Online Document 31

    14.7.1 Aluminum-centered neutral radicals

    R.F.C. Claridge

32. Online Document 32

    14.7.2 Aluminum-centered anion radicals

    R.F.C. Claridge

33. Online Document 33

    14.8.1 Gallium-centered neutral radicals

    R.F.C. Claridge

34. Online Document 34

    14.8.2 Gallium-centered radical anions

    R.F.C. Claridge

35. Online Document 35

    14.9.1 Cation radicals

    R.F.C. Claridge

36. Online Document 36

    15.1 Introduction

    C.C. Rowlands, R.D. Farley

37. Online Document 37

    15.2.1 Hydrocarbon radical anions

    C.C. Rowlands, R.D. Farley

38. Online Document 38

    15.2.2 Substituted compounds

    C.C. Rowlands, R.D. Farley

39. Online Document 39

    15.3.1 Oxygen containing heterocycles

    C.C. Rowlands, R.D. Farley

40. Online Document 40

    15.3.2 Nitrogen containing heterocycles

    C.C. Rowlands, R.D. Farley

41. Online Document 41

    15.3.3 Sulphur containing heterocycles

    C.C. Rowlands, R.D. Farley

42. Online Document 42

    15.3.4 Phosphorus containing heterocycles

    C.C. Rowlands, R.D. Farley

43. Online Document 43

    15.3.5 Selenium and tellurium containing heterocycles

    C.C. Rowlands, R.D. Farley

44. Online Document 44

    15.3.6 Heterocycles with two or more different heteroatoms

    C.C. Rowlands, R.D. Farley

45. Online Document 45

    15.4 Anion radicals from nitro compounds

    C.C. Rowlands, R.D. Farley

46. Online Document 46

    15.5.1 Esters and thioesters

    C.C. Rowlands, R.D. Farley

47. Online Document 47

    15.5.2 Aldehydes, ketones and their thio analogs

    C.C. Rowlands, R.D. Farley

48. Online Document 48

    15.5.3 Semidiones

    C.C. Rowlands, R.D. Farley

49. Online Document 49

    15.5.4 Acid anhydrides and derivatives

    C.C. Rowlands, R.D. Farley

50. Online Document 50

    15.6.1 Aliphatic azoalkenes

    C.C. Rowlands, R.D. Farley

51. Online Document 51

    15.6.2 Benzo[c]cinnolines and azobenzene derivatives

    C.C. Rowlands, R.D. Farley

52. Online Document 52

    15.6.3 Arylazophosphonates

    C.C. Rowlands, R.D. Farley

53. Online Document 53

    15.6.4 Bidiazines

    C.C. Rowlands, R.D. Farley

54. Online Document 54

    15.6.5 Tetrazines

    C.C. Rowlands, R.D. Farley

55. Online Document 55

    15.7.1 Sulphides and sulphones

    C.C. Rowlands, R.D. Farley

56. Online Document 56

    15.7.2 Imines and imides

    C.C. Rowlands, R.D. Farley

57. Online Document 57

    15.7.3 Fullerenes

    C.C. Rowlands, R.D. Farley

58. Online Document 58

    15.7.4 Tetracyanoquinodimethanes

    C.C. Rowlands, R.D. Farley

59. Online Document 59

    15.7.5 Phenylcarbonitriles

    C.C. Rowlands, R.D. Farley

60. Online Document 60

    15.7.6 Phosphaalkenes

    C.C. Rowlands, R.D. Farley

61. Online Document 61

    Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 1 · 15.7.7 Silanes

    C.C. Rowlands, R.D. Farley