ライフサイエンスコーパス: antiferromagnetically

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1 Co(II) neighbors and the other half coupled antiferromagnetically.

2 (Bz)(3), the metal atoms are found to couple antiferromagnetically.

3 netically while the x components are coupled antiferromagnetically.

4 ra reveal that the intermediate possesses an antiferromagnetically (AF) coupled Fe2(III/III) center w

5 Int-1 is a high-spin (S(1) = 5/2) Fe(III) antiferromagnetically (AF) coupled to an S(2) = 1/2 radi

6 erromagnetism arises from the canting of the antiferromagnetically aligned spins by the Dzyaloshinski

7 change-mediated ferromagnetic sheets coupled antiferromagnetically along the out-of-plane direction.

8 h do not play a role in gap formation, order antiferromagnetically at 2.5 K.

9 s Curie-like at high temperatures and orders antiferromagnetically at low temperatures.

10 ties of a spin-frustrated ground state of an antiferromagnetically coupled 3-fold symmetric trinuclea

11 ter has idealized C2h symmetry with a planar antiferromagnetically coupled [Fe(III)4(mu3-N)2]6+ core

12 f approximately 62 kJ/mol, to give H2 and an antiferromagnetically coupled [LNi(I)2](-) species.

13 ed by an S = 1/2 EPR signal indicative of an antiferromagnetically coupled [S = 5/2 Fe(III)/S = 2 Fe(

14 (mu-S)]2(2-) (4) with two {Fe(NO)}(7) motifs antiferromagnetically coupled and [(SH)2Fe(mu-S)]2(2-) (

15 wherein symmetrically bridged complexes are antiferromagnetically coupled and asymmetrically bridged

16 tains one type 1, one type 2, and a strongly antiferromagnetically coupled binuclear Cu(II)-Cu(II) ty

17 ) ions confirms the formation of one or more antiferromagnetically coupled clusters of Fe(3+) ions.

18 is state is best represented as a localized, antiferromagnetically coupled Co(IV)2 dimer.

19 he magnetic reversal and domain structure in antiferromagnetically coupled Co/Pt multilayers that are

20 tudies formulate neutral Cu corroles with an antiferromagnetically coupled Cu(II) corrole radical cat

21 ecies this HF mixing is also required for an antiferromagnetically coupled description of the two Cu(

22 mediate was detected and determined to be an antiferromagnetically coupled diferrous-dinitrosyl (S =

23 ect spectroscopic evidence that hDOHH has an antiferromagnetically coupled diiron center with histidi

24 ent with the same spectral properties as the antiferromagnetically coupled diiron(III) cluster in the

25 heir Mossbauer spectra suggest that both are antiferromagnetically coupled diiron(III) clusters.

26 in strong applied fields show that 2b is an antiferromagnetically coupled diiron(IV) center.

27 s complex is an open-shell singlet, with two antiferromagnetically coupled electrons residing on the

28 EPR spectra demonstrate the presence of an antiferromagnetically coupled Fe(III)Fe(II) center in Fe

29 complex active-site cofactor comprising two antiferromagnetically coupled ferric iron ions (Fe(3+)),

30 [4,4](3+) has an antiferromagnetically coupled ground state in which one

31 e class Ia E. coli beta2 contains dinuclear, antiferromagnetically coupled iron centers and one tyros

32 l of the data are consistent with 2 being an antiferromagnetically coupled iron(IV)-oxo pi-cation-rad

33 This species features two antiferromagnetically coupled ligand-centered radicals a

34 generation in a heterostructure composed of antiferromagnetically coupled magnetic layers.

35 own that the cofactor of R2lox represents an antiferromagnetically coupled Mn(III)/Fe(III) dimer link

36 Antiferromagnetically coupled Mn(III)Mn(IV) dimers have

37 ribonucleotide reductases (RNR) contains an antiferromagnetically coupled mu-oxo bridged diiron clus

38 as-isolated enzyme, the cluster contains an antiferromagnetically coupled pair of high-spin Fe(III)

39 delta = 0.62 +/- 0.02 mm/s) indicative of an antiferromagnetically coupled peroxodiferric complex.

40 c EPR signal consistent with formation of an antiferromagnetically coupled radical-copper complex.

41 w that the diamagnetic Fe-O-Fe unit contains antiferromagnetically coupled S = 1 Fe(IV) sites; diamag

42 etically for a triangular-lattice model with antiferromagnetically coupled S = 1/2 spins.

43 ronic structure methods were used to examine antiferromagnetically coupled spin states and correspond

44 which are blind to important diamagnetic or antiferromagnetically coupled states.

45 istent with pairs of high-spin iron(II) ions antiferromagnetically coupled through a dianionic AdN6Ad

46 d one four-coordinate iron, which are weakly antiferromagnetically coupled through a mu-1,3 carboxyla

47 d one four-coordinate iron, which are weakly antiferromagnetically coupled through mu-1,3-carboxylate

48 ng from two high-spin Fe(III) centers weakly antiferromagnetically coupled through the bridging imido

49 (and [1Cr]) to have a d(4) Cr configuration antiferromagnetically coupled to (dadi)(2-)*, and [1Fe]

50 involving a high-spin (S = 52) Fe(3+) center antiferromagnetically coupled to a (S = 1) NO(-) anion,

51 mposed of a Mo3Fe cluster with spin S(a) = 2 antiferromagnetically coupled to a 4Fe' cluster with spi

52 d as intermediate-spin iron(III) (SFe = 3/2) antiferromagnetically coupled to a chelate radical anion

53 (imino)pyridine radical anion (S(PDI) = 1/2) antiferromagnetically coupled to a high spin ferrous ion

54 t in this case the S(Fe) = 2 metal center is antiferromagnetically coupled to a ligand-centered radic

55 ive species to be a high-spin Fe(III) center antiferromagnetically coupled to an imido-based radical

56 tion with a low spin ferric center (S = 1/2) antiferromagnetically coupled to an imidyl radical (S(im

57 ido is best described as a high-spin Fe(III) antiferromagnetically coupled to an iminyl radical, affo

58 described as a high spin ferrous iron (S=2) antiferromagnetically coupled to an NO radical (S=1/2) [

59 (low to intermediate spin) ferric compounds antiferromagnetically coupled to bis(imino)pyridine radi

60 copy established high spin ferrous compounds antiferromagnetically coupled to chelate radical anions.

61 all four iron ions are high-spin ferric and antiferromagnetically coupled to form a diamagnetic S =

62 Tyr122, and the two iron sites are high-spin antiferromagnetically coupled to give a total 1/2 net sp

63 high-spin iron(II) centers that are strongly antiferromagnetically coupled to give rise to a singlet

64 best described in terms of Fe(III) (S = 5/2) antiferromagnetically coupled to NO(-) (S = 1).

65 [FeO(2)](8) corresponds to Fe(III) (S = 5/2) antiferromagnetically coupled to O(2)(-) (S = 1/2), and,

66 n, Co, and Ni complexes, the S = 1 ligand is antiferromagnetically coupled to the metal.

67 t suggested that VA.+ was equally ferro- and antiferromagnetically coupled to the oxoferryl moiety.

68 resulting from two Fe(III) (S = 5/2) centers antiferromagnetically coupled to yield an S = 0 ground s

69 that holochromodulin is shown to possess an antiferromagnetically coupled trinuclear assembly which

70 here the Mn(2+) and Mn(3+) ions are strongly antiferromagnetically coupled up to high temperatures.

71 The biferrous sites are all weakly antiferromagnetically coupled with mu-1,3 carboxylate br

72 indicate that the two Co(II) ions in AAP are antiferromagnetically coupled yielding an S = 0 ground s

73 rdinate (5C) ferrous centers that are weakly antiferromagnetically coupled, consistent with a mu-1,3

74 The two ptC strips are antiferromagnetically coupled, even though the edge Cu a

75 The data demonstrate the formation of an antiferromagnetically coupled, high-spin diiron(III/III)

76 hows that the irons of the diferric site are antiferromagnetically coupled, implying a single-atom, p

77 ess O(2) or H(2)O(2) and the formation of an antiferromagnetically coupled, valence-localized, high-s

78 NO(-) and an Fe(3+) center that are strongly antiferromagnetically coupled.

79 d [2Fe-2S] Rieske-type center are moderately antiferromagnetically coupled.

80 ating that the two Fe(III) ions are strongly antiferromagnetically coupled.

81 valent high-spin (Sloc = 2) sites, which are antiferromagnetically coupled; its quadrupole splitting

82 N2V(III) core and where each vanadium center antiferromagnetically couples to give a ground state sin

83 Both compounds order antiferromagnetically despite the lack of obvious supere

84 The chains appear to be antiferromagnetically exchange coupled, giving cusps in

85 lar forms of Abeta(1-40) with Cu(2+) contain antiferromagnetically exchange-coupled binuclear Cu(2+)

86 perconductor with properties as expected for antiferromagnetically mediated superconductivity.

87 ds emerges when charge carriers are added to antiferromagnetically ordered CuO(2) layers.

88 per oxides, superconductivity arises when an antiferromagnetically ordered phase has been suppressed

89 In the antiferromagnetically ordered state, the electronic-spec

90 After preparing a nonequilibrium antiferromagnetically ordered state, we observe relaxati

91 ow 50 K, Sr(3)Co(2)O(4)Cl(2) adopts a canted antiferromagnetically ordered state.

92 The Os(VI) ions order antiferromagnetically with a propagation vector k = (1/2

93 108 K, while the high-spin Co(II) ions order antiferromagnetically with a propagation vector k = (1/2

94 crystallinity, the two compounds are ordered antiferromagnetically with susceptibility maxima at 26 a

95 The ligand-centered radical couples antiferromagnetically with the Fe center.

96 at are reintroduced into the interface align antiferromagnetically with the magnetization at first sc

97 tra Mn atoms occupying Ga sites and coupling antiferromagnetically with the rest of the Mn atoms.

98 , and nearest-neighbor Co(2+) moments couple antiferromagnetically within the CoO(2) planes.

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