Aerosol Jet Printing of a Benzocyclobutene-Based Ink as Adhesive Material for Wafer Bonding Application

Aerosol jet printing (AJP) is an emerging additive manufacturing technology that is gaining increasing attention in the electronic field. Several studies have been carried out on the AJP of conductive, semiconductive, and dielectric polymers for electronic applications. However, wafer bonding is an application that is still uncovered by literature. Therefore, in this work, the AJP of benzocyclobutene (BCB) as a polymeric adhesive for wafer bonding is presented for the first time. A thorough characterization of the processing parameters is carried out to identify the most ideal conditions for printing at a relatively high speed. Then, square patterns are printed, proving the versatility of the AJP technology in terms of the reachable thickness of the deposited BCB patterns. Complex patterns with a resolution of approximate to 60 mu m are also printed. The bonding properties of the BCB are characterized from a morphological and mechanical point of view. In particular, the shear strength of the BCB coatings deposited with AJP is approximate to 39 MPa and it is comparable with the shear strength of BCB coating deposited by spin-coating. Consequently, AJP represents a valid alternative for the deposition of polymeric adhesive for wafer bonding

Phosphorus recovery from a pilot-scale grate furnace: influencing factors beyond wet chemical leaching conditions

Phosphorus is a non-renewable resource going to exhaustion in the future. Sewage sludge ash is a promising secondary raw material due to its high phosphorus content. In this work, the distribution of 19 elements in bottom and cyclone ashes from pilot-scale grate furnace have been monitored to determine the suitability for the phosphorus acid extraction. Moreover, the influence of some parameters beyond wet chemical leaching conditions were investigated. Experimental results showed that bottom ash presented lower contamination in comparison to cyclone ash and low co-dissolution of heavy metals (especially Cr, Pb and Ni), while high phosphorus extraction efficiencies (76-86%) were achieved. High Al content in the bottom ash (9.4%) negatively affected the phosphorus extraction efficiency as well as loss on ignition, while the particle size reduction was necessary for ensuring a suitable contact surface. The typology of precipitating agents did not strongly affect the phosphorus precipitation, while pH was the key parameter. At pH 3.5-5, phosphorus precipitation efficiencies higher than 90% were achieved, with a mean phosphorus content in the recovered material equal to 16-17%, comparable to commercial fertilizers. Instead, the co-precipitation of Fe and Al had a detrimental effect on the recovered material, indicating the need for additional treatments

Sampling Mechanism for Low Gravity Bodies

In future exploration missions to low gravity bodies (e.g. a Mars moon or a near-Earth asteroid) it is planned to collect more than 100 grams of soil and return them to Earth. In previous studies several sampling tools have been proposed but there is no single sampling technology for low-gravity bodies that has been specifically conceived to provide the ability to collect material in any envisaged situation. Low gravity bodies present indeed peculiar conditions which need to be taken into account during the design and test of sampling and sample handling systems. Primarily, the very reduced gravity limits the thrust reaction capability in support to drilling operations; and, although reactions can be achieved by spacecraft anchoring or by thrust reversal, these operative conditions could limit the effectiveness of the sampling action. An alternative solution is the exploitation of the forces naturally arising from Spacecraft momentum inversion, which can be achieved by ‘touch and go’ techniques (as e.g. performed in Hayabusa mission). Although the small duration of the contact with the soil would anyhow limit the sampling depth and the collectable soil types, a properly designed sampling system would require to conclude the operation with a great effectiveness. In the last three years an ESA founded study has been carried on and a fully functional sampling mechanism for "touch and go" sampling on a low-gravity body has been selected, designed and breadboarded. Based on the results of several Proof-Of-Principle models tested on different types of specimen and after the analysis performed on a dynamic simulation model for the sampling action, a device implementing the most promising sampling technique has been designed and manufactured. It has been then tested under ambient conditions using various kinds of asteroid soil stimulants. The proposed paper will resume the key aspects and the main achievements of the study

Stereoselective Synthesis of α,α’-Dihydroxy-β,β’-diaryl-β-amino Acids by Mannich-like Condensation of Hydroarylamides

Dual \u3b1,\u3b1\u2019-Dihydroxy-\u3b2-amino acids are very interesting tools for several industrial applications. Nevertheless, few derivatives are reported in the literature concerning the substitution pattern as well as their enantioselective syntheses are lacking. Here, we report on the preparation of enantiopure \u3b1,\u3b1\u2019-dihydroxy-\u3b2,\u3b2\u2019-diaryl-\u3b2-amino acid (dual) derivatives by an efficient Mannich-like condensation of hydroarylamides with 5,6-diethoxy-5,6-dimethyl-1,4-dioxan-2-one (triethylsilyl)ketene acetal. The synthetic protocol has been optimized affording the dual compounds in very good yields and with different aryl substitution patterns. Taking advantage of the \u201cdouble stereodifferentiation\u201d concept, a highly stereoselective reaction was performed: of the 16 possible isomers, only two diastereoisomers (d.r. up to 93:7) formed. Insights on the high stereocontrol of this condensation were given

Tetrahydro-4H-(pyrrolo[3,4-d]isoxazol-3-yl)methanamine : a bicyclic diamino scaffold stabilizing parallel turn conformations

Tetrahydro-4H-(pyrrolo[3,4-d]isoxazol-3-yl)methanamine scaffold was designed as diamino derivative to stabilize parallel turn conformations. Its synthesis took advantage of a [1,3]-dipolar cycloaddition reaction between the nitrile oxide derived from the inexpensive enantiopure L-phenylalanine, and N-benzyl-3-pyrroline. Two diastereoisomers were formed whose distribution depends on the selected base. 3aR,6aS-Isomer is favoured in organic bases which formation is driven by pi-interactions. On the other hand, the above interactions were significantly prevented using an inorganic base due to the chaotropic effect of the cation, decreasing the amount of the above isomer. Finally, we demonstrated that this isomer is able of stabilizing parallel turn conformations when inserted in short peptide sequences

A Non-coded β2,2-Amino Acid with Isoxazoline Core Able to Stabilize Peptides Folding through an Unprecedented Hydrogen Bond

Dedicated to Prof. Cesare Gennari on the occasion of his 70th birthday New peptidomimetics containing a beta(2,)(2)-isoxazoline amino acid, i.e. 5-(aminomethyl)-3-phenyl-4,5-dihydroisoxazole-5-carboxylic acid (Isox-beta(2,)(2)AA), were prepared and studied by NMR and theoretical calculation. Although similar amino acid derivatives have already been prepared via 1,3-dipolar cycloaddition reaction, neither experimental details nor characterization were found and they were never used for peptide synthesis. Both enantiomers were inserted in peptide sequences to verify their ability to induce a secondary structure. We found that an unexpected conformation is given by R-Isox-beta(2,)(2)AA, inducing the folding of short peptides thanks to an unprecedented H-bond involving C=N of the isoxazoline side chain of our beta(2,)(2)-AA

Ctr-1 Mets7 motif inspiring new peptide ligands for Cu(i)-catalyzed asymmetric Henry reactions under green conditions

Taking inspiration from the Ctr-1 Mets7 Cu(i) binding motif, effective hybrid catalysts have been developed for asymmetric Henry condensations under green conditions. The introduction of an unnatural dipeptide mimic allowed to increase the catalytic performance. Metal transporters' binding domains could be exploited as a strategy for designing hybrid catalysts for homogeneous catalysis

Rational design of a user-friendly aptamer/peptide-based device for the detection of staphylococcus aureus

The urgent need to develop a detection system for Staphylococcus aureus, one of the most common causes of infection, is prompting research towards novel approaches and devices, with a particular focus on point-of-care analysis. Biosensors are promising systems to achieve this aim. We coupled the selectivity and affinity of aptamers, short nucleic acids sequences able to recognize specific epitopes on bacterial surface, immobilized at high density on a nanostructured zirconium dioxide surface, with the rational design of specifically interacting fluorescent peptides to assemble an easy-to-use detection device. We show that the displacement of fluorescent peptides upon the competitive binding of S. aureus to immobilized aptamers can be detected and quantified through fluorescence loss. This approach could be also applied to the detection of other bacterial species once aptamers interacting with specific antigens will be identified, allowing the development of a platform for easy detection of a pathogen without requiring access to a healthcare environment

MediaChrom: exploring a new family of pyrimidoindolone-based polarity-sensitive dyes

The modern biological research asks for a continuous development of new fluorescent dyes characterized by improved performances and suitable to be used as markers or probes [1]. A particular class of dyes, called polarity-sensitive dyes have the unique features to display a different emission maximum as a function of the polarity of their molecular environment (media). This peculiarity makes polarity-sensitive dyes the ideal probes to monitor the local properties of particular cell districts as well as different type of biomolecular interactions [2]. Since many years, we have been interested in the development of new strategies for the synthesis and the functionalization of indoles and polycyclic indole-based heterocycles. In this context, we reported a domino approach to pyrimidoindolones [3] that displayed interesting fluorescence properties. Starting from these findings, a small library of original polarity-sensitive fluorescent dyes, nicknamed MediaChrom, has been prepared [4]. They are characterized by a pyrimidoindolone core fitted out with a conjugated push-pull system, and a linker for an easy coupling with biomolecules. The synthetic strategy involves a highly chemo- and regioselective gold catalyzed cycloisomerization as key step. The photophysical properties of MediaChrom dyes have been evaluated, and some potential biological applications have been spottily investigated. [1] Lakowicz, J. R. Principles of Fluorescence Spectroscopy, 3rd ed.; Springer: New York, 2006. [2] Klymchenko, A. S.; Mely, Y. In: Progress in Molecular Biology and Translational Science, Morris, M.C. Editor(s), Academic Press, 2013, Vol. 113, Cap. 2, 35. [3] Facoetti, D.; Abbiati, G.; d\u2019Avolio, L.; Ackermann, L.; Rossi, E. Synlett 2009, 2273. [4] Dell'Acqua, M.; Ronda, L.; Piano, R.; Pellegrino, S.; Clerici, F.; Rossi, E.; Mozzarelli, A.; Gelmi, M. L.; Abbiati, G. J. Org. Chem. 2015, 21, 10939. This work has been supported by Fondazione Cariplo, Grant No. 2012-0907

Constraints on the χ_(c1) versus χ_(c2) polarizations in proton-proton collisions at √s = 8 TeV

The polarizations of promptly produced χ_(c1) and χ_(c2) mesons are studied using data collected by the CMS experiment at the LHC, in proton-proton collisions at √s=8  TeV. The χ_c states are reconstructed via their radiative decays χ_c → J/ψγ, with the photons being measured through conversions to e⁺e⁻, which allows the two states to be well resolved. The polarizations are measured in the helicity frame, through the analysis of the χ_(c2) to χ_(c1) yield ratio as a function of the polar or azimuthal angle of the positive muon emitted in the J/ψ → μ⁺μ⁻ decay, in three bins of J/ψ transverse momentum. While no differences are seen between the two states in terms of azimuthal decay angle distributions, they are observed to have significantly different polar anisotropies. The measurement favors a scenario where at least one of the two states is strongly polarized along the helicity quantization axis, in agreement with nonrelativistic quantum chromodynamics predictions. This is the first measurement of significantly polarized quarkonia produced at high transverse momentum