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Single case cognitive neuropsychological investigations involve the precise characterization of cognitive impairment at the level of an individual participant. This deep data precision affords a more fine-grained understanding of the cognitive and neural underpinnings of complex tasks, and continues to provide unique insights that inform theory in cognitive neuroscience. Here, we present a single case study of an individual, F.R., who suffered a stroke that led to chronic reading and writing problems that include an impairment to the orthographic working memory system proposed to be involved in both written language production and comprehension. Individuals who have been previously reported with a similar cognitive impairment commonly have left parietal lesions. However, F.R.'s orthographic working memory deficit resulted from damage to the right cerebellum, specifically to a region that is both structurally and functionally connected to the left parietal lobe and has been identified as part of the spelling network in previous meta-analyses of writing fMRI studies. From this lesion-symptom association, we argue that orthographic working memory is subserved by a cortical-cerebellar circuit, with damage at any point in the circuit resulting in an impairment to this function. Such a conclusion is warranted by observations from this single case approach, and we argue that these observations would likely have been missed if F.R. had been included in a larger, shallower group study. In addition to elucidating our understanding of the neural basis of spelling, this case study demonstrates the value that single case neuropsychology can continue to bring to cognitive neuroscience.

Women of reproductive age who are drinking alcohol and not using effective contraception are at-risk for an alcohol-exposed pregnancy, which could result in a child with a fetal alcohol spectrum disorder (FASD). Nurses are an important partner in addressing at-risk alcohol use. It is imperative for alcohol education to be incorporated into nursing curricula so that future nurses have the tools to identify at-risk alcohol use. Three universities have worked together to create Fetal Alcohol Spectrum Disorders: A Toolkit. This toolkit was designed for nurses to facilitate the recognition and prevention of FASD and address gaps that exists around alcohol use.

The structural, electronic, magnetic and theoretical study of the complex [Co3(HL)2(μ-AcO)2(AcO)2], 1, (HL is the dianion obtained by deprotonation of N,N’-bis(salicylidene)-2-hydroxy-1,3-propanediamine and AcO is acetate) shows that 1 crystallizes with two independent molecules in the asymmetric unit. Each molecule is a trinuclear complex. Both molecules have similar geometry, and correspond to a spin system based on trapped mixed valences on six-coordinate metal centres, CoIII(s=0)-CoII(s=3/2)-CoIII(s=0). The rigid framework formed by the tetradentate Salen-type ligands HL and the syn-syn bridging acetate anions is a characteristic feature observed in other related complexes. However, the here reported compound is the first one in this family having Z’>1. UV-Vis spectrum shows a broad band in the visible region where d-d transition for ions CoIII and CoII are. EPR spectra and the electronic energy estimations of the ground state show the presence of two conformers s=3/2. The χMT product at 300 K is 3.24 emu mol−1K per trinuclear unit, this product is expected for CoII where the contribution of orbital angular moment is taken into account (3.38 emu mol−1K for L=3).

Three novel branched polyamines N,N,N’,N’-tetrakis-[3((pyridine-2-methyl)-amine) propyl]-1,4- butanediamine (1), N,N,N’,N’-tetrakis-[N-((2-methylpyridine)ethyl)propanamide]ethylenediamine (2) and N,N,N’,N’-tetrakis-[3((2-hidroxibenziliden)-amine)propyl]-1,4-butanediamine (3), were synthesized starting from 2-pyridinecarboxaldeyde with DAB-Am-4 for 1, PAMAM G0 for 2 and from salicylaldehyde with DAB-Am-4 for 3. The pathway reactions have been proposed by 1H-NMR, IR and Atomic Absorption Spectroscopy. The optimal reaction time was set by IR spectroscopy following aldehyde peak modification. 1 and 2 were obtained as both hydrochlorides and as free amines and 3 only as free imine. These polyamines were characterized by UV-Vis, IR, 1H-NMR and 13C-NMR and Mass Spectrometry.

Synthesis, structural, electronic, and magnetic characterization of two [CuII 2(thb)] (thb = N,N,N’,N’- tetrakis-{3-[(2- hydroxibenzyliden)-amine]propyl}-1,4-butanodiamine)]) crystalline phases (1a and 1b) are reported. Both, 1a and 1b, showed free radical scavenging activity, which was quantified by the DPPH free radical scavenging activity assay. 1b crystallized in a P21/c space group. In 1b each molecule contains two CuII-(hidroxibenzyliden) groups bonded in the extremes of the organic DAB-Am nucleus. The CuII-(hidroxibenzyliden) groups of each extreme, form 1D chains along of the b-axis. IR and UV-Vis spectra showed d-d transitions and νCu-O, νCu-N vibrations respectively, confirming the formation of the compound. 1H-NMR spectra of 1a and 1b showed similar spectra, being characteristics of paramagnetic compounds. Bulk magnetization of 1a and 1b from 2 K to 300 K showed paramagnetic behaviour. The best fit for the susceptibility data was obtained using Curie-Weiss and modified Curie-Weiss equations with θ and C values of θ1a/1b C-W = 0 ± 1K, C1a/1b C-W = 0.82/0.66 cm3 K mol-1, and θ1a/1b modified C-W = 0.6 ± 1K and C1a/1b modified C-W = 0.80/0.70 cm3 K mol-1. The X-band ESR spectra of 1a and 1b in solid samples showed a single and a rhombic signals, respectively, with g values around 2.1 at 77 K and 300 K, however, in CH2Cl2 solutions at 77 K the spectra were similar. The spectroscopic and magnetic results allowed us to conclude that 1a and 1b are two different crystalline phases which were proven to act as effective antioxidants showing both an IC50 = 16.5 μM, in contrast with Trolox, IC50 = 39.3 μM, normally used as a vitamin E analog and a strong antioxidant. Additionaly the DPPH free radical is scavened by reduction mechanism of CuII to CuI. The overall electronic, magnetic and structural information about 1a and 1b provide us some characteristics of this kind of transitional metal ionic coordination compounds.