Roberto Paolesse

Prof. Roberto Paolesse

Department of Chemical Science and Technologies University of Rome Tor Vergata
orcid

Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 October 2016 in Chemical Reviews
Verified
Journal Article
Open access
Roberto PaolesseRoberto Paolesse
Roberto Paolesse
SNSara Nardis
Sara Nardis
DMDonato Monti
Donato Monti
MSManuela Stefanelli
Manuela Stefanelli
Corrado Di NataleCorrado Di Natale
Corrado Di Natale
Porphyrins and related macrocycles have been intensively exploited as sensing materials in chemical sensors, since in these devices they mimic most of their biological functions, such as reversible binding, catalytic activation, and optical changes. Such a magnificent bouquet of properties allows applying porphyrin derivatives to different transducers, ranging from nanogravimetric to optical devices, also enabling the realization of multifunctional chemical sensors, in which multiple transduction mechanisms are applied to the same sensing layer. Potential applications are further expanded through sensor arrays, where cross-selective sensing layers can be applied for the analysis of complex chemical matrices. The possibility of finely tuning the macrocycle properties by synthetic modification of the different components of the porphyrin ring, such as peripheral substituents, molecular skeleton, coordinated metal, allows creating a vast library of porphyrinoid-based sensing layers. From among these, one can select optimal arrays for a particular application. This feature is particularly suitable for sensor array applications, where cross-selective receptors are required. This Review briefly describes chemical sensor principles. The main part of the Review is divided into two sections, describing the porphyrin-based devices devoted to the detection of gaseous or liquid samples, according to the corresponding transduction mechanism. Although most devices are based on porphyrin derivatives, seminal examples of the application of corroles or other porphyrin analogues are evidenced in dedicated sections.

1 September 2003 in Biosensors and Bioelectronics
Verified
Journal Article
Closed access
Corrado Di NataleCorrado Di Natale
Corrado Di Natale
Antonella MacagnanoAntonella Macagnano
Antonella Macagnano
EMEugenio Martinelli
Eugenio Martinelli
Roberto PaolesseRoberto Paolesse
Roberto Paolesse
GDGiuseppe D'Arcangelo
Giuseppe D'Arcangelo
ADArnaldo D'Amico
Arnaldo D'Amico

1 May 2014 in Analytica Chimica Acta
Verified
Journal Article
Closed access
Corrado Di NataleCorrado Di Natale
Corrado Di Natale
Roberto PaolesseRoberto Paolesse
Roberto Paolesse
EMEugenio Martinelli
Eugenio Martinelli
RCRosamaria Capuano
Rosamaria Capuano

1 May 2010 in Lung Cancer
Verified
Journal Article
Closed access
ADArnaldo D’aMico
Arnaldo D’aMico
Giorgio PennazzaGiorgio Pennazza
Giorgio Pennazza
Marco SantonicoMarco Santonico
Marco Santonico
EMEugenio Martinelli
Eugenio Martinelli
CRClaudio Roscioni
Claudio Roscioni
Corrado Di NataleCorrado Di Natale
Corrado Di Natale

1 January 1999 in Chemical Communications
Verified
Journal Article
Closed access
PDF file
Roberto PaolesseRoberto Paolesse
Roberto Paolesse
SMSonia Mini
Sonia Mini
FSFrancesco Sagone
Francesco Sagone
TBTristano Boschi
Tristano Boschi
LJLaurent Jaquinod
Laurent Jaquinod
KSKevin M Smith
Kevin M Smith
One-pot synthesis of 5,10,15-triphenylcorrole has been achieved by reaction of benzaldehyde with an excess of pyrrole; the triphenylphosphinocobalt complex of 5,10,15-triphenylcorrole has been structurally characterized using X-ray crystallography.

28 December 2000 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
Roberto PaolesseRoberto Paolesse
Roberto Paolesse
SNSara Nardis
Sara Nardis
FSFrancesco Sagone
Francesco Sagone
RKRichard G. Khoury
Richard G. Khoury