22 research outputs found
Supplemental Material - Practice—Not Task Difficulty—Mediated the Focus of Attention Effect on a Speed-Accuracy Tradeoff Task
Supplemental Material for Practice—Not Task Difficulty—Mediated the Focus of Attention Effect on a Speed-Accuracy Tradeoff Task by Masahiro Yamada, Keith R. Lohse, Christopher Rhea, Randy J. Schmitz, and Louisa D. Raisbeck in Perceptual and Motor Skills.</p
Interlayer Interaction of Two-Dimensional Layered Spin Crossover Complexes [Fe<sup>II</sup>H<sub>3</sub>L<sup>Me</sup>][Fe<sup>II</sup>L<sup>Me</sup>]X (X<sup>-</sup> = ClO<sub>4</sub><sup>-</sup>, BF<sub>4</sub><sup>-</sup>, PF<sub>6</sub><sup>-</sup>, AsF<sub>6</sub><sup>-</sup>, and SbF<sub>6</sub><sup>-</sup>; H<sub>3</sub>L<sup>Me</sup> = Tris[2-(((2-methylimidazol-4-yl)methylidene)amino)ethyl]amine)
A series of two-dimensional (2D) spin crossover complexes, [FeIIH3LMe][FeIILMe]X (X- = ClO4-, BF4-, PF6-, AsF6-,
SbF6-) 1−5, have been synthesized, where H3LMe denotes an hexadentate N6 tripodlike ligand containing three
imidazole groups, tris[2-(((2-methylimidazol-4-yl)methylidene)amino)ethyl]amine. Compounds 1−5 exhibit a two-step (HS-[FeIIH3LMe]2+ + HS-[FeIILMe]-) ↔ (HS-[FeIIH3LMe]2+ + LS-[FeIILMe]-) ↔ (LS-[FeIIH3LMe]2+ + LS-[FeIILMe]-)
spin-transition. The crystal structure of [FeIIH3LMe][FeIILMe]PF6 (3) was determined at 295, 200, and 100 K. The
structure consists of homochiral extended 2D puckered sheets, in which the complementary [FeIIH3LMe]2+ and [FeIILMe]-
capped tripodlike components, linked together by imidazole−imidazolate hydrogen bonds, are alternately arrayed
in an up-and-down mode. The Fe−N bond distances and angles revealed that the FeII sites of both constituting
units are in the high-spin (HS) state at 295 K; at 200 K, the FeII sites of [FeIIH3LMe]2+ and [FeIILMe]- are in the HS
and low-spin (LS) states, respectively. The FeII sites of both constituting units are in the LS state at 100 K. The
size of the counteranion affects significantly the intra- and interlayer interactions leading to modifications of the
spin crossover behavior. The onset of the second spin-transition of the ClO4- (1) and BF4- (2) salts adjoins the
first spin-transition, while a mixed (HS-[FeIIH3LMe]2+ + LS-[FeIILMe]-) spin-state spans a temperature range as wide
as 70 K for salts 3−5 with larger counteranions, PF6-, AsF6-, and SbF6-, respectively. Compounds 1 and 2
showed remarkable LIESST (light induced excited spin state trapping) and reverse-LIESST effects, whereas 3−5
showed no remarkable LIESST effect. The interlayer interaction due to the size of the counteranion is an important
factor governing the spin crossover behavior and LIESST effect
sj-docx-1-tej-10.1177_20417314221114616 – Supplemental material for Rapid and efficient generation of cartilage pellets from mouse induced pluripotent stem cells by transcriptional activation of BMP-4 with shaking culture
Supplemental material, sj-docx-1-tej-10.1177_20417314221114616 for Rapid and efficient generation of cartilage pellets from mouse induced pluripotent stem cells by transcriptional activation of BMP-4 with shaking culture by Maolin Zhang, Kunimichi Niibe, Takeru Kondo, Phoonsuk Limraksasin, Hiroko Okawa, Xinchao Miao, Yuya Kamano, Masahiro Yamada, Xinquan Jiang and Hiroshi Egusa in Journal of Tissue Engineering</p
A 2D Layered Spin Crossover Complex Constructed by NH···Cl<sup>-</sup> Hydrogen Bonds: [Fe<sup>II</sup>H<sub>3</sub>L<sup>Me</sup>]Cl·I<sub>3</sub> (H<sub>3</sub>L<sup>Me</sup> = Tris[2-(((2-methylimidazoyl-4-yl)methylidene)amino)ethyl]amine
A 2D layered spin crossover complex, [FeIIH3LMe]Cl·I3, has been synthesized from the reaction of FeIIICl3, a tripod
ligand (H3LMe = tris[2-(((2-methylimidazoyl-4-yl)methylidene)amino)ethyl]amine), and NaI in methanol. The compound
showed an abrupt spin transition between the HS (S = 2) and LS (S = 0) states at T1/2 = 110 K without hysteresis.
The crystal structures of the HS and LS states were determined at 180 and 90 K. A 2D layered structure is
composed of NH···Cl- hydrogen bonds between the Cl- ion and three neighboring imidazole groups of [FeIIH3LMe]2+.
The green light irradiation at 5 K induced the LIESST effect, and the thermal relaxation process from the HS to LS
state showed a sigmoid curve at T > 55 K
A New Family of Spin Crossover Complexes with a Tripod Ligand Containing Three Imidazoles: Synthesis, Characterization, and Magnetic Properties of [Fe<sup>II</sup>H<sub>3</sub>L<sup>Me</sup>](NO<sub>3</sub>)<sub>2</sub>·1.5H<sub>2</sub>O, [Fe<sup>III</sup>L<sup>Me</sup>]·3.5H<sub>2</sub>O, [Fe<sup>II</sup>H<sub>3</sub>L<sup>Me</sup>][Fe<sup>II</sup>L<sup>Me</sup>]NO<sub>3</sub>, and [Fe<sup>II</sup>H<sub>3</sub>L<sup>Me</sup>][Fe<sup>III</sup>L<sup>Me</sup>](NO<sub>3</sub>)<sub>2</sub> (H<sub>3</sub>L<sup>Me</sup> = Tris[2-(((2-methylimidazol-4-yl)methylidene)amino)ethyl]amine)
A new family of spin crossover complexes, [FeIIH3LMe](NO3)2·1.5H2O (1), [FeIIILMe]·3.5H2O (2), [FeIIH3LMe][FeIILMe]NO3 (3), and [FeIIH3LMe][FeIIILMe](NO3)2 (4), has been synthesized and characterized, where H3LMe denotes a
hexadentate N6 tripod ligand containing three imidazole groups, tris[2-(((2-methylimidazol-4-yl)methylidene)amino)ethyl]amine. It was found that the spin and oxidation states of the iron complexes with this tripod ligand are tuned
by the degree of deprotonation of the imidazole groups and by the 2-methyl imidazole substituent. Magnetic
susceptibility and Mössbauer studies revealed that 1 is an HS-FeII complex, 2 exhibits a spin equilibrium between
HS and LS-FeIII, 3 exhibits a two-step spin transition, where the component [FeIILMe]- with the deprotonated ligand
participates in the spin transition process in the higher temperature range and the component [FeIIH3LMe]2+ with the
neutral ligand participates in the spin transition process in the lower temperature range, and 4 exhibits spin transition
of both the FeII and FeIII sites. The crystal structure of 3 consists of homochiral extended 2D puckered sheets, in
which the capped tripodlike components [FeIIH3LMe]2+ and [FeIILMe]- are alternately arrayed in an up-and-down
mode and are linked by the imidazole−imidazolate hydrogen bonds. Furthermore, the adjacent 2D homochiral
sheets are stacked in the crystal lattice yielding a conglomerate as confirmed by the enantiomeric circular dichorism
spectra. Compounds 3 and 4 showed the LIESST (light induced excited spin state trapping) and reverse-LIESST
effects upon irradiation with green and red light, respectively
Titanium Nanosurface with a Biomimetic Physical Microenvironment to Induce Endogenous Regeneration of the Periodontium
The periodontium
supports the teeth by dentoalveolar fibrous joints
that serve unique oral functions. Endogenous regeneration of the periodontium
around artificial teeth (dental implants) provides a cost-effective
solution for the extension of healthy life expectancy but remains
a challenge in regenerative medicine. Biomimetics can create smart
biomaterials that tune endogenous cells at a tissue–material
interface. Here, we created a smart titanium nanosurface mimicking
the surface nanotopography and micromechanical properties of the tooth
root cementum (TRC), which is essential for the induction of dentoalveolar
fibrous joints to regenerate the periodontium. After transplantation
into the rat renal capsule, only the titanium artificial tooth with
the TRC-mimetic nanosurface formed a complex dentoalveolar fibrous
joint structure, with bone tissue, periodontal ligament (PDL), and
TRC, in the decellularized jawbone matrix. TRC-mimetic titanium implants
induce the formation of functional periodontium, even in a jawbone
implantation model, which generally causes osseointegration (ankyloses).
In human PDL cells, TRC analogousness in the surface mechanical microenvironment
regulates matrix mineralization through bone sialoprotein expression
and phosphorus metabolism, which are critical for cementogenesis.
Therefore, the titanium nanosurfaces with nanotopographical and mechanical
microenvironments mimicking the TRC surface induce dentoalveolar fibrous
joints for periodontal regeneration by interfacial tuning of endogenous
cells
Association between time from concussion and SD Max Vel.
Data showing no association between the number of days since the concussion event and neuromotor performance as assessed with SD Max Vel.</p
Data processing and model specification flow chart.
Abbreviations: HS = head shake, EC = Eyes-closed conditions. (A) Flow chart of the data processing. The two boxes in the bottom are the sample size submitted for the statistical analyses for all variables except CV Stride time. *1 n = the number of subjects, nt = the number of trials. *2 for CV stride time, n = 138 healthy and n = 61 concussed participants for the EC condition and n = 141 healthy and n = 60 concussed participants for the HS condition were submitted for analyses. (B) the model specification process: Fixed effects coefficients are B0, B1, B2, and B3, j = j-th group of i-th individual. u0i represents the random effect of the individual intercept, and e0i represents the residuals, where both are assumed to be normally distributed.</p
Smartphone app.
(A) Placement of the phone on the thigh and the illustration of stepping movement. (B) Representative time series of the thigh flexion angle in the sagittal plane during the stepping in place task. (C) Study design and dependent variables extracted from the smartphone app.</p
