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1.
J Fluoresc ; 2024 May 16.
Article in English | MEDLINE | ID: mdl-38753256

ABSTRACT

A 4-amino-1,8-naphthalimide containing tetramethylpiperidine in N-position was synthesized. The prepared 1,8-naphthalimide was found to possess bright yellow-green fluorescence in a solid state, which could be switched-off in the presence of acid vapors and then switched-on after exposure on base vapors. The observed fluorescence quenching or enhancement, respectively, was more than 10-fold. This behavior was quite opposite to that of the similar 4-oxy-1,8-naphthalimide, in which a well-pronounced PET process operates. In addition, the observed fluorescence quenching was accompanied with color change from yellow to red. Based on these results, the reported 4-amino-1,8-naphthalimide was successfully applied as a reversible solid-state emissive chemosensing material for rapid detection of acid-base vapors for multiple usage.

2.
Molecules ; 28(17)2023 Aug 29.
Article in English | MEDLINE | ID: mdl-37687156

ABSTRACT

The rapid progress in the field of fluorescent probes and fluorescent sensing material extended this research area toward more complex molecular logic gates capable of carrying out a variety of sensing functions simultaneously. These molecules are able to calculate a composite result in which the analysis is not performed by a man but by the molecular device itself. Since the first report by de Silva of AND molecular logic gate, all possible logic gates have been achieved at the molecular level, and currently, utilization of more complicated molecular logic circuits is a major task in this field. Comparison between two digits is the simplest logic operation, which could be realized with the simplest logic circuit. That is why the right understanding of the applied principles during the implementation of molecular digital comparators could play a critical role in obtaining logic circuits that are more complicated. Herein, all possible ways for the construction of comparators on the molecular level were discussed, and recent achievements connected with these devices were presented.

3.
Molecules ; 28(8)2023 Apr 21.
Article in English | MEDLINE | ID: mdl-37110865

ABSTRACT

The synthesis, sensor activity, and logic behavior of a novel 4-iminoamido-1,8-naphthalimide bichromophoric system based on a "fluorophore-receptor" architecture with ICT chemosensing properties is reported. The synthesized compound showed good colorimetric and fluorescence signaling properties as a function of pH and proved itself as a promising probe for the rapid detection of pH in an aqueous solution and base vapors in a solid state. The novel dyad is able to work as a two-input logic gate with chemical inputs H+ (Input 1) and HO- (Input 2) executing INHIBIT logic gate. The synthesized bichromophoric system and the corresponding intermediates demonstrated good antibacterial activity toward Gram (+) and Gram (-) bacteria when compared with the Gentamycin standard.


Subject(s)
Fluorescent Dyes , Naphthalimides , Naphthalimides/chemistry , Anti-Bacterial Agents/pharmacology , Hydrogen-Ion Concentration
4.
Pharmaceuticals (Basel) ; 16(3)2023 Mar 01.
Article in English | MEDLINE | ID: mdl-36986481

ABSTRACT

Over the last few years, the development of fluorescent probes has received considerable attention. Fluorescence signaling allows noninvasive and harmless real-time imaging with great spectral resolution in living objects, which is extremely useful for modern biomedical applications. This review presents the basic photophysical principles and strategies for the rational design of fluorescent probes as visualization agents in medical diagnosis and drug delivery systems. Common photophysical phenomena, such as Intramolecular Charge Transfer (ICT), Twisted Intramolecular Charge Transfer (TICT), Photoinduced Electron Transfer (PET), Excited-State Intramolecular Proton Transfer (ESIPT), Fluorescent Resonance Energy Transfer (FRET), and Aggregation-Induced Emission (AIE), are described as platforms for fluorescence sensing and imaging in vivo and in vitro. The presented examples are focused on the visualization of pH, biologically important cations and anions, reactive oxygen species (ROS), viscosity, biomolecules, and enzymes that find application for diagnostic purposes. The general strategies regarding fluorescence probes as molecular logic devices and fluorescence-drug conjugates for theranostic and drug delivery systems are discussed. This work could be of help for researchers working in the field of fluorescence sensing compounds, molecular logic gates, and drug delivery.

5.
J Fluoresc ; 33(1): 43-51, 2023 Jan.
Article in English | MEDLINE | ID: mdl-36208369

ABSTRACT

Ace naphthene as a primary material was nitrated and further reacted by various processes such as oxidation, imidation and amination in order to obtain dyad 5. The dyad 5 fluoresces in solvents of different polarity and the emission is shifted bathochromically with increasing the solvent polarity due to ICT enhancement, The fluorescent enhancement is greatest in case of chloroform (ФF = 0.48) on excitation at 420 nm,The influences of the pH on dyad 5 were also investigated, The results can be considered as representing off-on-off states. Dyad 5 executes two input XNOR logic gates, towards H+ and HO- ions, "off-on-off" switching behavior between H+ and HO- ions was observed, The synthesized compounds were tested for antimicrobial activity of Gram-positive and Gram-negative bacteria, The compounds tested have a good antibacterial activity as compared with standard compound (Gentamycin).

6.
Molecules ; 27(21)2022 Nov 04.
Article in English | MEDLINE | ID: mdl-36364383

ABSTRACT

A novel highly water-soluble 1,8-naphthalimide with pH and viscosity-sensing fluorescence was synthesized and investigated. The synthesized compound was designed as a molecular device in which a molecular rotor and molecular "off-on" switcher were integrated. In order to obtain a TICT driven molecular motion at C-4 position of the 1,8-naphthalimide fluorophore, a 4-methylpiperazinyl fragment was introduced. The molecular motion was confirmed after photophysical investigation in solvents with different viscosity; furthermore, the fluorescence-sensing properties of the examined compound were investigated in 100% aqueous medium and it was found that it could be used as an efficient fluorescent probe for pH. Due to the non-emissive deexcitation nature of the TICT fluorophore, the novel system showed low yellow-green emission, which represented "power-on"/"rotor-on" state. The protonation of the methylpiperazine amine destabilized the TICT process, which was accompanied by fluorescence enhancement indicating a "power-on"/"rotor-off" state of the system. The results obtained clearly illustrated the great potential of the synthesized compound to serve as pH- and viscosity-sensing material in aqueous solution.


Subject(s)
Fluorescent Dyes , Naphthalimides , Naphthalimides/chemistry , Fluorescent Dyes/chemistry , Viscosity , Water , Hydrogen-Ion Concentration
7.
Molecules ; 27(13)2022 Jun 30.
Article in English | MEDLINE | ID: mdl-35807479

ABSTRACT

A new highly water-soluble 1,8-naphthalimide fluorophore designed on the "fluorophore-spacer-receptor1-receptor2" model has been synthesized. Due to the unusually high solubility in water, the novel compound proved to be a selective PET-based probe for the determination of pHs in aqueous solutions and rapid detection of water content in organic solvents. Based on the pH dependence of the probe and its high water solubility, the INH logic gate was achieved using NaOH and water as chemical inputs, where NaOH is the disabler and the water is an enabler. In addition, the probe showed effective fluorescence "off-on" reversibility on glass support after exposure to acid and base vapors, which defines it as a promising platform for rapid detection of acid/base vapors in the solid-state, thus extending the molecular sensing concept from solution to the solid support.


Subject(s)
Fluorescent Dyes , Naphthalimides , Fluorescent Dyes/chemistry , Naphthalimides/chemistry , Sodium Hydroxide , Solvents/chemistry , Water/chemistry
8.
J Fluoresc ; 32(1): 405-417, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34988841

ABSTRACT

A novel simple molecular chemosensor 2 was synthesized and examined for pH, cations and anions detection. At pH values higher than 10, probe 2 switches on a green emission where the excited state intramolecular proton transfer (ESIPT) is ceased. Also, the probe absorption spectrum shows a clear pH dependence, and the probe aqueous solution (ethanol/water = 1:2, borate buffer) responds selectively and sensitively through its fluorescence spectrum to the presence of Cu2+. Job's plot gave a 2:1 stoichiometry of Probe-2/Cu2+ complex, which responds to the presence of S2- and H2PO4- in aqueous solution (ethanol/water = 1:2, borate buffer) by its absorption and fluorescence spectra. In addition, probe 2 mimics a digital comparator based on three INHIBIT logic gates by different outputs using HO- and H+ as inputs. Moreover, probe 2 also executes AND and NOT TRANSFER logic gates using Cu2+ and S2- as inputs.

9.
J Fluoresc ; 29(6): 1431-1443, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31760584

ABSTRACT

We reported here the unique ability of a Rhodamine 6G-based probe (3) to detect discriminately several targets, including H+, HO-, Cu2+, Hg2+, Fe3+, Co2+, Cd2+, Zn2+, Sn2+, Ni2+, Al3+, Pb2+, Ce3+and Ag+, by unambiguously colorimetric and fluorimetric outcomes. In aqueous solutions, the presence of proton induced the ring-opening of rhodamine moiety but the presence of hydroxide induced the conversion of 2-hydroxyphenyl hydrazone moiety from the non-fluorescent benzenoid form into the fluorescent quinoid form. The probe could to distinguish between different cations in DMF and to work like an artificial tongue at molecular level. Several logic gates including OR, INHIBIT and TRANSFER, were performed by the probe. Moreover, the probe is able to execute three INHIBIT logic gates by two inputs, which was exploited to execute a digital molecular comparator.

10.
Spectrochim Acta A Mol Biomol Spectrosc ; 223: 117304, 2019 Dec 05.
Article in English | MEDLINE | ID: mdl-31255861

ABSTRACT

A novel rhodamine-pyrazole based molecular probe was designed and easily synthesized. The probe could to detect several analytes in aqueous solution at biological pH (HEPES, pH = 7.2). Several heavy metal cations, including Cu2+, Fe3+, Al3+, Hg2+ and Ni2+ were detected discriminately by the probe. Also, the novel compound exhibited a good sensory selectivity towards S2O52- by both absorption and emission spectra. Moreover, probe/Cu2+ complex could to detect several anions, including F-, CN-, S2-, CH3COO-, CO32- and NO2-. Furthermore, the probe exhibited a high potential to work as a molecular system able to perform a number of logical operations such as AND, NAND, NOR and INHIBIT logic gates.

11.
Article in English | MEDLINE | ID: mdl-29433042

ABSTRACT

A novel fluorescence sensing 1,8-naphthalimide fluorophore is synthesized and investigated. The novel probe comprising two different binding moieties is capable to detect selectively Fe3+ over the other representative metal ions as well as a combination of biologically important cations such as Fe3+, Cu2+ and Hg2+ in the physiological range without an interfering effect of the pHs. Due to the remarkable fluorescence changes in the presence of Fe3+, Hg2+ and Cu2+ ions, INH and AND logic gates are executed and the system is able to act as a single output combinatorial logic circuit with three chemical inputs.

12.
Article in English | MEDLINE | ID: mdl-28432919

ABSTRACT

Two novel highly water-soluble fluorescence sensing 1,8-naphthalimides are synthesized and investigated. The novel compounds are designed on the "fluorophore-receptor1-spacer-receptor2" model as a molecular fluorescence probe for determination of cations and anions in 100% aqueous media. The novel probes comprising N-imide and N-phenylpiperazine or morpholine substituents are capable to operate simultaneously via ICT and PET signaling mechanism as a function of pH and to recognize selectively Cu2+ and Hg2+ over the other representative metal ions. Due to the remarkable fluorescence changes in the presence of protons, hydroxyl anions, Hg2+ and Cu2+, INH and doubly disabled INH logic gates are executed and the systems are able to act as a single output combinatorial logic circuit with four chemical inputs.

13.
J Fluoresc ; 26(3): 1091-100, 2016 May.
Article in English | MEDLINE | ID: mdl-27048224

ABSTRACT

A novel PAMAM dendron designed as a wavelength-shifting bichromophore with 1,8-naphthalimide energy "donor" capable of absorbing light and efficiently transferring the energy to a focal Rhodamine 6G "acceptor" was synthesized and investigated. Moreover, the system was configured on the "fluorophore-spacer-receptor" format. Thus, the distinguishing features of FRET systems were successfully combined with the properties of photoinduced electron transfer and classical ring-opening sensor systems. The synthesized compound shows excellent signaling properties towards protons, Hg(2+) and Fe(3+) ions, therefore, the system is able to act as an one-output combinatorial logic circuit with four chemical inputs.

14.
Mater Sci Eng C Mater Biol Appl ; 51: 7-15, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25842102

ABSTRACT

Novel biocompatible water-soluble fluorescent micelles with embedded perylene diimides (PDI) for intracellular applications have been prepared by self assembling of amphiphilic poly(vinyl alcohol)-b-poly(acrylonitrile) (PVA-b-PAN) copolymers in the presence of synthesized fluorophores. Amphiphilic PVA-b-PAN copolymers were obtained by selective hydrolysis of well-defined poly(vinyl acetate)-b-poly(acrylonitrile) (PVAc-b-PAN) copolymer. The preparation of the novel fluorescence micelles consisting of PVA hydrophilic shell and PAN hydrophobic core with incorporated PDI fluorophores has been confirmed by DLS and TEM analysis. The cytotoxicity of the water-soluble fluorophores and their internalization into living cells depending on the micellar concentration have been tested. It was shown that they could successfully enter in living cells without destroying their morphology. The results obtained indicate that the novel water-soluble fluorescent micelles with embedded PDI fluorophores would be suitable for potential intracellular biomedical applications.


Subject(s)
Delayed-Action Preparations/chemistry , Fluorescent Dyes/chemistry , Imides/chemistry , Imides/toxicity , Nanocapsules/chemistry , Perylene/analogs & derivatives , Water/chemistry , 3T3 Cells , Animals , Cell Survival/drug effects , Delayed-Action Preparations/therapeutic use , Fluorescent Dyes/toxicity , Mice , Micelles , Nanocapsules/toxicity , Nanocapsules/ultrastructure , Particle Size , Perylene/chemistry , Perylene/toxicity , Solubility , Subcellular Fractions/chemistry
15.
ACS Nano ; 9(4): 4200-9, 2015 Apr 28.
Article in English | MEDLINE | ID: mdl-25769194

ABSTRACT

A tailored optimization of perovskite solar cells requires a detailed understanding of the processes limiting the device efficiency. Here, we study the role of the hole transport layer (HTL) spiro-MeOTAD and its thickness in a mesoscopic TiO2-based solar cell architecture. We find that a sufficiently thick (200 nm) HTL not only increases the charge carrier collection efficiency but also the light harvesting efficiency. This is due to an enhanced reflection of a smooth HTL/Au-electrode interface. The rough CH3NH3PbI3 perovskite surface requires an HTL thickness of >400 nm to avoid surface recombination and guarantee a high open-circuit voltage. Analyses of the electroluminescence efficiency and the diode ideality factor show that the open-circuit voltage becomes completely limited by trap-assisted recombination in the perovskite for a thick HTL. Thus, spiro-MeOTAD is a very good HTL choice from the device physics' point of view. The fill factor analyzed by the Suns-Voc method is not transport limited, but trap-recombination limited as well. Consequently, a further optimization of the device has to focus on defects in the polycrystalline perovskite film.

16.
Spectrochim Acta A Mol Biomol Spectrosc ; 135: 792-800, 2015 Jan 25.
Article in English | MEDLINE | ID: mdl-25150429

ABSTRACT

A novel PAMAM wavelength-shifting bichromophoric system has been successfully developed. Novel compound was configured as a light harvesting antenna where the system surface is labeled with yellow-green emitting 4-(N,N-dimethylamino)ethylamino-1,8-naphthalimide "donor" units capable of absorbing light and efficiently transferring the energy to a focal Rhodamine 6G "acceptor". The periphery of the system was designed on the "fluorophore-spacer-receptor" format, capable of acting as a molecular fluorescence photoinduced electron transfer based probe. Due to the both effects, photoinduced electron transfer in the periphery of the system and pH dependent rhodamine core absorption, novel antenna is able to act as a selective ratiometric pH fluorescence probe in aqueous medium. Thus, the distinguishing features of the fluorescence resonance energy transfer systems were successfully combined with the properties of classical ring-opening charge transfer systems, which may be beneficially for monitoring pH variations in complex samples.


Subject(s)
Dendrimers/chemistry , Fluorescent Dyes/chemistry , Light , Absorption, Physicochemical , Cations , Dendrimers/chemical synthesis , Electrons , Fluorescence , Hydrogen-Ion Concentration , Metals/chemistry , Naphthalimides/chemistry , Rhodamines/chemistry
17.
J Fluoresc ; 24(6): 1621-8, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25199470

ABSTRACT

A novel blue-emitting 1,8-naphthalimide fluorophore designed as a molecular PET-based probe for determination of pH and detection of transition metal ions in the environment was successfully synthesized. Novel compound was configured on the "fluorophore-spacer-receptor" format. Due to the tertiary amine receptor the novel system showed "off-on" switching properties under the transition from alkaline to acid media (FE = 3.2) and in the presence of Zn(2+) ions (FE = 2.5). The results obtained illustrate the high potential of the synthesized blue-emitting 1,8-naphthalimide fluorophore as an efficient pH chemosensing material and a selective probe for Zn(2+) ions.


Subject(s)
Biosensing Techniques , Electrons , Fluorescent Dyes/chemistry , Light , Molecular Probes , Naphthalimides/chemistry , Naphthalimides/pharmacology , Zinc/analysis , Electron Transport , Hydrogen-Ion Concentration , Magnetic Resonance Spectroscopy , Molecular Structure , Protons , Spectroscopy, Fourier Transform Infrared
18.
Bioorg Med Chem ; 21(21): 6292-302, 2013 Nov 01.
Article in English | MEDLINE | ID: mdl-24075142

ABSTRACT

Herein we report on the synthesis and sensor activity of a novel pH sensitive probe designed as highly water-soluble fluorescent micelles by grafting of 1,8-naphthalimide-rhodamine bichromophoric FRET system (RNI) to the PMMA block of a well-defined amphiphilic diblock copolymer-poly(methyl methacrylate)-b-poly(methacrylic acid) (PMMA48-b-PMAA27). The RNI-PMMA48-b-PMAA27 adduct is capable of self-assembling into micelles with a hydrophobic PMMA core, containing the anchored fluorescent probe, and a hydrophilic shell composed of PMAA block. Novel fluorescent micelles are able to serve as a highly sensitive pH probe in water and to internalize successfully HeLa and HEK cells. Furthermore, they showed cell specificity and significantly higher photostability than that of a pure organic dye label such as BODIPY. The valuable properties of the newly prepared fluorescent micelles indicate the high potential of the probe for future biological and biomedical applications.


Subject(s)
Fluorescent Dyes/chemistry , Micelles , Nanoparticles/chemistry , Cell Survival/drug effects , Fluorescence Resonance Energy Transfer , Fluorescent Dyes/chemical synthesis , Fluorescent Dyes/toxicity , HEK293 Cells , HeLa Cells , Humans , Hydrogen-Ion Concentration , Hydrophobic and Hydrophilic Interactions , Naphthalimides/chemical synthesis , Naphthalimides/chemistry , Polymethacrylic Acids/chemical synthesis , Polymethacrylic Acids/chemistry , Polymethacrylic Acids/toxicity , Rhodamines/chemical synthesis , Rhodamines/chemistry , Water/chemistry
19.
J Fluoresc ; 23(3): 459-71, 2013 May.
Article in English | MEDLINE | ID: mdl-23397487

ABSTRACT

Herein we report on the design, divergent synthesis and photophysical behavior of novel PAMAM light-harvesting dendrons from first and second generation. The surface of novel compounds is labeled with 4-alkylamino-1,8-naphthalimide yellow-green emitting "donor" fluorophores capable of absorbing light and efficiently transferring the energy to a single rhodamine "acceptor" dye. Due to the pH dependent rhodamine absorption the novel systems show "off-on" switching energy transfer mechanism from alkaline to acid media. The results obtained illustrate the high potential of the synthesized wavelength-shifting fluorophores as efficient pH chemosensing materials.

20.
Article in English | MEDLINE | ID: mdl-22842131

ABSTRACT

An ester terminated dihydroimidazonaphthalimide as multi-functional logic device is presented. Due to the optical changes as a function of pH this simple molecule is able to act as a molecular pH metre, a digital comparator and a half-adder. It was demonstrated that the dihydroimidazonaphthalimide comparator could be used as a fundamental element of an optical device for control of pH windows. Also, the ability of the device to detect metal ions in DMF and in water/DMF (3:1, v/v) at different pHs has been evaluated by monitoring the changes of its fluorescence intensity. Among the tested metal ions (Cd(2+), Co(2+), Cu(2+), Fe(3+), Ni(2+), Pb(2+), Zn(2+), Bi(3+), Hg(2+) and Ag(+)) only Fe(3+) and Bi(3+) were efficiently detected. In water/DMF (3:1, v/v) XOR and XNOR logic gates are presented using pH and Fe(3+) as chemical inputs based on encoding binary digits of logical conventions.


Subject(s)
Electrons , Esters/chemistry , Light , Naphthalimides/chemistry , Absorption , Cations , Coloring Agents/chemistry , Dimethylformamide/chemistry , Hydrogen-Ion Concentration , Metals/chemistry , Solutions , Spectrometry, Fluorescence , Water/chemistry
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