7 research outputs found
EUROSENSORS XVII : book of abstracts
Fundação Calouste Gulbenkien (FCG).Fundação para a Ciência e a Tecnologia (FCT)
Non-covalent interactions in organotin(IV) derivatives of 5,7-ditertbutyl- and 5,7-diphenyl-1,2,4-triazolo[1,5-a]pyrimidine as recognition motifs in crystalline self- assembly and their in vitro antistaphylococcal activity
Non-covalent interactions are known to play a key role in biological compounds due to their
stabilization of the tertiary and quaternary structure of proteins [1]. Ligands similar to purine rings,
such as triazolo pyrimidine ones, are very versatile in their interactions with metals and can act as
model systems for natural bio-inorganic compounds [2]. A considerable series (twelve novel
compounds are reported) of 5,7-ditertbutyl-1,2,4-triazolo[1,5-a]pyrimidine (dbtp) and 5,7-diphenyl-
1,2,4-triazolo[1,5-a]pyrimidine (dptp) were synthesized and investigated by FT-IR and 119Sn
M\uf6ssbauer in the solid state and by 1H and 13C NMR spectroscopy, in solution [3]. The X-ray
crystal and molecular structures of Et2SnCl2(dbtp)2 and Ph2SnCl2(EtOH)2(dptp)2 were described, in
this latter pyrimidine molecules are not directly bound to the metal center but strictly H-bonded,
through N(3), to the -OH group of the ethanol moieties. The network of hydrogen bonding and
aromatic interactions involving pyrimidine and phenyl
rings in both complexes drives their self-assembly. Noncovalent
interactions involving aromatic rings are key
processes in both chemical and biological recognition,
contributing to overall complex stability and forming
recognition motifs. It is noteworthy that in
Ph2SnCl2(EtOH)2(dptp)2 \u3c0\u2013\u3c0 stacking interactions between
pairs of antiparallel triazolopyrimidine rings mimick basepair
interactions physiologically occurring in DNA (Fig.1).
M\uf6ssbauer spectra suggest for Et2SnCl2(dbtp)2 a
distorted octahedral structure, with C-Sn-C bond angles
lower than 180\ub0. The estimated angle for Et2SnCl2(dbtp)2
is virtually identical to that determined by X-ray diffraction. Ph2SnCl2(EtOH)2(dptp)2 is
characterized by an essentially linear C-Sn-C fragment according to the X-ray all-trans structure.
The compounds were screened for their in vitro antibacterial activity on a group of reference
staphylococcal strains susceptible or resistant to methicillin and against two reference Gramnegative
pathogens [4] . We tested the biological activity of all the specimen against a group of
staphylococcal reference strains (S. aureus ATCC 25923, S. aureus ATCC 29213, methicillin
resistant S. aureus 43866 and S. epidermidis RP62A) along with Gram-negative pathogens (P.
aeruginosa ATCC9027 and E. coli ATCC25922). Ph2SnCl2(EtOH)2(dptp)2 showed good
antibacterial activity with a MIC value of 5 \u3bcg mL-1 against S. aureus ATCC29213 and also
resulted active against methicillin resistant S. epidermidis RP62A
An Exploration of the Metal Dependent Selectivity of a Metalloporphyrins Coated Quartz Microbalances Array
Several studies in the last two decades have demonstrated that metalloporphyrins coated quartz microbalances can be fruitfully used in many diverse applications, spanning from medical diagnosis to environmental control. This large versatility is due to the combination of the flexibility of metalloporphyrins molecular design with the independence of the quartz microbalance signal from the interaction mechanisms. The nature of the metal atom in the metalloporphyrins is often indicated as one of the most effective tools to design differently selective sensors. However, the properties of sensors are also strongly affected by the characteristics of the transducer. In this paper, the role of the metal atom is investigated studying the response, to various volatile compounds, of six quartz microbalance sensors that are based on the same porphyrin but with different metals. Results show that, since quartz microbalances (QMB) transducers can sense all the interactions between porphyrin and volatile compounds, the metal ion does not completely determine the sensor behaviour. Rather, the sensors based on the same molecular ring but with different metal ions show a non-negligible common behaviour. However, even if limited, the different metals still confer peculiar properties to the sensors and might drive the sensor array identification of the pool of tested volatile compounds
An exploration of the metal dependent selectivity of a metalloporphyrins coated quartz microbalances array
Several studies in the last two decades have demonstrated that metalloporphyrins coated quartz microbalances can be fruitfully used in many diverse applications, spanning from medical diagnosis to environmental control. This large versatility is due to the combination of the flexibility of metalloporphyrins molecular design with the independence of the quartz microbalance signal from the interaction mechanisms. The nature of the metal atom in the metalloporphyrins is often indicated as one of the most effective tools to design differently selective sensors. However, the properties of sensors are also strongly affected by the characteristics of the transducer. In this paper, the role of the metal atom is investigated studying the response, to various volatile compounds, of six quartz microbalance sensors that are based on the same porphyrin but with different metals. Results show that, since quartz microbalances (QMB) transducers can sense all the interactions between porphyrin and volatile compounds, the metal ion does not completely determine the sensor behaviour. Rather, the sensors based on the same molecular ring but with different metal ions show a non negligible common behaviour. However, even if limited, the different metals still confer peculiar properties to the sensors and might drive the sensor array identification of the pool of tested volatile compounds. © 2016 by the authors; licensee MDPI, Basel, Switzerland
An Exploration of the Metal Dependent Selectivity of a Metalloporphyrins Coated Quartz Microbalances Array
Several studies in the last two decades have demonstrated that metalloporphyrins coated quartz microbalances can be fruitfully used in many diverse applications, spanning from medical diagnosis to environmental control. This large versatility is due to the combination of the flexibility of metalloporphyrins molecular design with the independence of the quartz microbalance signal from the interaction mechanisms. The nature of the metal atom in the metalloporphyrins is often indicated as one of the most effective tools to design differently selective sensors. However, the properties of sensors are also strongly affected by the characteristics of the transducer. In this paper, the role of the metal atom is investigated studying the response, to various volatile compounds, of six quartz microbalance sensors that are based on the same porphyrin but with different metals. Results show that, since quartz microbalances (QMB) transducers can sense all the interactions between porphyrin and volatile compounds, the metal ion does not completely determine the sensor behaviour. Rather, the sensors based on the same molecular ring but with different metal ions show a non-negligible common behaviour. However, even if limited, the different metals still confer peculiar properties to the sensors and might drive the sensor array identification of the pool of tested volatile compounds