ライフサイエンスコーパス: antiferromagnetically

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

2 netically while the x components are coupled antiferromagnetically.

3 angements, with ferromagnetic chains coupled antiferromagnetically.

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

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

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

7 imaging the phase-coexistence of regions of antiferromagnetically (AFM) ordered and fully aligned sp

8 scattering of the hexagonal LuMnO(3) in the antiferromagnetically (AFM) ordered state.

9 The Pt magnetic moments induced by the antiferromagnetically aligned FeCo and Gd moments are me

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

11 iscent of the spin wave of strongly coupled, antiferromagnetically aligned spins on a square lattice.

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

13 ly ordered internally and the layers coupled antiferromagnetically along the stacking direction.

14 e trisradical tricationic complexes interact antiferromagnetically and form a one-dimensional Heisenb

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

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

17 oposed that the AAF ligand singly reduces to antiferromagnetically couple to the palladium(I) complex

18 itional electron on neighboring p-terphenyls antiferromagnetically couple.

19 a high-spin Fe(III) center which is strongly antiferromagnetically coupled (J = -524 cm(-1)) to an im

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

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

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

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

24 ly ordered along the edges of the ribbon and antiferromagnetically coupled across its width(1,2,5).

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

26 wherein symmetrically bridged complexes are antiferromagnetically coupled and asymmetrically bridged

27 1,4,8,11-tetraazacyclotetradecane) featuring antiferromagnetically coupled anisotropic Mn(III) ions.

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

29 at 11 K due to the layers being bridged and antiferromagnetically coupled by the nonmagnetic cyanide

30 dimer, known as Kremer's dimer, contains two antiferromagnetically coupled chromium(III) metal ions a

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

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

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

34 trongly favor a dinuclear mu-oxo-bridged and antiferromagnetically coupled complex, but which undergo

35 strongly favor a dinuclear u-oxo-bridged and antiferromagnetically coupled complex, but which undergo

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

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

38 nsistent with an assignment of Fe2/Fe6 as an antiferromagnetically coupled diferric pair.

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

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

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

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

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

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

45 The unexpected additive roles of the two antiferromagnetically coupled elements exemplify the imp

46 giant Dy(3) triangles sandwiching a strongly antiferromagnetically coupled Fe(18) ring, leading to a

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

48 f the Ir spacer thickness leads to synthetic antiferromagnetically coupled FePd layers, with an inter

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

50 [4,4](3+) has an antiferromagnetically coupled ground state in which one

51 in the oxygen-evolving complex, we identify antiferromagnetically coupled high-spin manganese center

52 ,Me))V}(2)(1,3-mu(2)-N(3))(2)] (6), with two antiferromagnetically coupled high-spin V(II) ions.

53 All neighboring spins are antiferromagnetically coupled in 1 and 2.

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

55 mance stems from a tetra-iron center with an antiferromagnetically coupled iron dimer on the hematite

56 t Fe-trimer nodes affecting reaction contain antiferromagnetically coupled iron species, and highligh

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

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

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

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

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

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

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

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

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

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

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

68 let diradical Ni(II)-catalysts featuring two antiferromagnetically coupled singlet diradical diamine

69 Antiferromagnetically coupled skyrmion sublattices are o

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

71 Symmetric ZGNRs typically show antiferromagnetically coupled spin-ordered edge states(1

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

73 The observed lattice is composed of three antiferromagnetically coupled sublattices, and each subl

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

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

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

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

78 s a singlet, where the Fe(IV) and Cu(II) are antiferromagnetically coupled through the H-bond between

79 ters feature a local high-spin Fe(3+) center antiferromagnetically coupled to (3) [NO](-) .

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

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

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

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

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

85 iate spin (S = 1) cobalt(III) center that is antiferromagnetically coupled to a ligand-centered radic

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

87 s species support a high-spin Fe(III) center antiferromagnetically coupled to a superoxide ligand, si

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

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

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

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

92 be consistent with an S = 1 Fe(IV)=O that is antiferromagnetically coupled to an S = 1/2 radical delo

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

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

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

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

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

98 dense to provide local spin moments that are antiferromagnetically coupled to Ni spins.

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

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

101 = solvent), where an S = 1 Co(III) center is antiferromagnetically coupled to S = 1/2 TAML(*+), which

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

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

104 the nearest W-site magnetic moments that are antiferromagnetically coupled to the V magnetic moments

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

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

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

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

109 However, the systems examined are antiferromagnetically coupled with |J/D| > 1.

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

111 which adjacent ferromagnetic monolayers are antiferromagnetically coupled(9).

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

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

114 o adjacent T-shaped metalloradicals that are antiferromagnetically coupled, giving an S=0 ground stat

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

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

117 The two anionic electrons in 2 are strongly antiferromagnetically coupled, thus in agreement with th

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

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

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

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

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

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

124 pin iron(I) center ( S(Fe) = 3/2) engaged in antiferromagnetically coupling with a ligand radical ani

125 Both compounds order antiferromagnetically despite the lack of obvious supere

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

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

128 perconductor with properties as expected for antiferromagnetically mediated superconductivity.

129 ndidate Cu(3)Zn(OH)(6)FBr, and another is an antiferromagnetically ordered compound EuCu(3)(OH)(6)Cl(

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

131 growth of correlations through coarsening of antiferromagnetically ordered domains(6).

132 ermodynamic and spectroscopic evidence of an antiferromagnetically ordered heavy-fermion ground state

133 monopoles on the holmium sublattice and the antiferromagnetically ordered iridium ions.

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

135 In the antiferromagnetically ordered state, the electronic-spec

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

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

138 k the system by characterizing high-fidelity antiferromagnetically ordered states and demonstrating q

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

140 108 K, while the high-spin Co(II) ions order antiferromagnetically with a propagation vector k = (1/2

141 d multilayers of CoB/Ir/Pt, coupled together antiferromagnetically with an Ir layer.

142 materials, denoted as MUV-1(M), which order antiferromagnetically with critical temperatures that de

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

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

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

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

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