Abstract Adolescence refers to the period of physical and psychological development between childhood and adulthood. The beginning of adolescence is loosely anchored to the onset of puberty, which brings dramatic alterations in hormone levels and a number of consequent physical changes. Puberty onset is also associated with profound changes in drives, motivations, psychology, and social life; these changes continue throughout adolescence. There is an increasing number of neuroimaging studies looking at the development of the brain, both structurally and functionally, during adolescence. Almost all of these studies have defined development by chronological age, which shows a strong—but not unitary—correlation with pubertal stage. Very few neuroimaging studies have associated brain development with pubertal stage, and yet there is tentative evidence to suggest that puberty might play an important role in some aspects of brain and cognitive development. In this paper we describe this research, and we suggest that, in the future, developmental neuroimaging studies of adolescence should consider the role of puberty. Hum Brain Mapp, 2010. © 2010 Wiley‐Liss, Inc.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
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Two series of random copolymers, poly(styrene-d8-co-4-vinylbenzamide) and poly(styrene-d8-co-4-vinyl-N-ethylbenzamide), were prepared with varying compositions. The functionalized random copolymers were tested for their abilities to reinforce the weak interface between immiscible polymers: polystyrene and poly(2-vinylpyridine). The effect of the hydrogen-bonding groups with different interaction strengths (primary or secondary benzamide) was studied through the evaluation of interfacial fracture toughness and fracture surface characteristics. For the compositions investigated, the copolymers with the primary benzamide functionality were shown to attain higher fracture toughness values than the substituted benzamide copolymers. Additionally, the composition at which maximum interfacial strengthening was attained was much lower in the primary benzamide case (fmax = 0.06) than in the substituted benzamide case (fmax = 0.25). However, in both cases the observed strengthening was lower than our previous results using copolymers bearing phenolic groups. The effect of the copolymer functionality, including such variables as steric constraints and degree of self-association, and composition drift on the measured interfacial properties are discussed.
Two new mutants of Rhodobacter sphaeroides deficient in sulfolipid accumulation were isolated by directly screening mutagenized cell lines for polar lipid composition by thin-layer chromatography of lipid extracts. A genomic clone which complemented the mutations in these two lines, but not the previously described sulfolipid-deficient sqdA mutant, was identified. Sequence analysis of the relevant region of the clone revealed three, in tandem open reading frames, designated sqdB, ORF2, and sqdC. One of the mutants was complemented by the sqdB gene, and the other was complemented by the sqdC gene. Insertional inactivation of sqdB also inactivated sqdC, indicating that sqdB and sqdC are cotranscribed. The N-terminal region of the 46-kDa putative protein encoded by the sqdB gene showed slight homology to UDP-glucose epimerase from various organisms. The 30-kDa putative protein encoded by ORF2 showed very striking homology to rabbit muscle glycogenin, a UDP-glucose utilizing, autoglycosylating glycosyltransferase. The 26-kDa putative protein encoded by the sqdC gene was not homologous to any protein of known function.
The rhodium and iridium complexes [(tBu2bpy)2M(μ-Cl)]2 (M = Rh (1), Ir (2)) containing the bidentate tBu2bpy (4,4′-di-tert-butyl-2,2′-bipyridyl) ligand were prepared. Dimeric complexes 1 and 2 react with HSiPh3 to give [(tBu2bpy)MH(SiPh3)(μ-Cl)]2 in good yields (M = Rh (3) 92%, Ir (4) 90%). Addition of PiPr3 to 3 or 4 gave monomeric crystalline complexes of the type (tBu2bpy)MH(SiPh3)Cl(PiPr3) (M = Rh (7) and Ir (8)), which adopt a slightly distorted octahedral coordination geometry with the tBu2bpy ligand occupying sites trans to the hydride and chloride ligands, as determined by X-ray crystallography. Salt metathesis reactions of 7 and 8 produced (tBu2bpy)MH(SiPh3)(R)PiPr3 as monomeric octahedral complexes with the tBu2bpy ligand occupying sites trans to the hydride and R substituents (M = Rh, R = H (11) and M = Ir, R = H (12), Me (14), and Ph (15)). Salt metathesis reactions with 3 and 4 also generated the dimeric, dicationic complexes [(tBu2bpy)M(SiPh3)(μ-H)]2[B(C6F5)4]2, where M = Rh (16) or Ir (17). Thermolysis of 15 at 100 °C in C6H6 for 1 day produced 12 and Ph4Si in 47% yield, and heating 15 in the presence of 1 equiv of HSiR3 (R = Ph, Et) also gave 12, as well as the Si−C coupled product PhSiR3 in >95% yield.
The preparation and characterization of new osmium(II) and osmium(IV) silyl derivatives containing the cyclopentadienyl(phosphine) and pentamethylcyclopentadienyl(phosphine) ligand sets are described. The osmium silyl complexes are prepared by thermal reactions of hydrosilanes with osmium(II) alkyl complexes of the type Cp'(PR3)2OsCH2SiMe3 (Cp' = Cp, R = Ph (4), Me (5); Cp' = η5-C5Me5, R = Me (7)), which in turn are available via alkylation of the corresponding bromo complexes. The synthesis of alkyl derivatives of Cp(PR3)2Os (R = Ph, Me) requires the use of dialkylmagnesium reagents, while alkylation of the more electron-rich Cp*(PMe3)2Os system can be achieved using Grignard reagents. Additionally, reaction of Cp(PPh3)2OsBr with AgOTf (Tf = SO2CF3) affords the osmium(II) triflate complex Cp(PPh3)2OsOTf (2), which possesses a labile triflate group. The structure of complex 2 was determined by X-ray crystallography. Similar to their ruthenium analogs, the osmium(II) alkyl complexes 4, 5, and 7 thermally activate arene C−H bonds. Reaction of 7 with HSiR2[S(p-Tol)] (R = S(p-Tol), Me) provides metallacycle complexes of the = S(p-Tol) (11), Me (13)) via activation of both the Si−H and arene C−H bonds in the silanes. The X-ray structure of 13 is described. Alkyl complexes 4, 5, and 7 react with HSiR2Cl (R = Ph, Me) to give osmium(II) silyl and/or osmium(IV) bis(silyl) hydride species, depending on the reaction conditions and the strength of the Os−P bond. Reaction of 7 with HSiMeCl2 or HSiCl3 affords, exclusively, the osmium(II) silyl derivatives. Exchange reactions at silicon are used to synthesize Cp*(PMe3)2OsSiMe2OTf (24) and Cp*(PMe3)2OsSiMe[S(p-Tol)]2 (25) from the corresponding chloro(silyl) complexes Cp*(PMe3)2OsSiMe2Cl (17) and Cp*(PMe3)2OsSiMeCl2 (18). The solution behavior and solid-state structure of 24 indicate that the compound may be described as a base-stabilized silylene complex.