Jung Y et al (2019) A wavelength-tunable and facilely functionable DA type naphthalene core skeleton: Synthesis, photophysical property, and bio-imaging applications for cells and tissues. Dyes Pigm 162:104–111
Nicolescu A et al (2020) Synthesis, photophysical properties and solvatochromic analysis of some naphthalene-1, 8-dicarboxylic acid derivatives. J Mol Liq 303:112626
Banerjee A et al (2012) A naphthalene exciplex based Al 3+ selective on-type fluorescent probe for living cells at the physiological pH range: experimental and computational studies. Analyst 137(9):2166–2175
[PMID:
22416274]
Mataga N, Tomura M, Nishimura H (1965) Fluorescence decay times of naphthalene and naphthalene excimers. Mol Phys 9(4):367–375
Benedetti E, Kocsis LS, Brummond KM (2012) Synthesis and photophysical properties of a series of cyclopenta [b] naphthalene solvatochromic fluorophores. J Am Chem Soc 134(30):12418–12421
[PMID:
22793873]
Oyama Y et al (2021) Advantages of naphthalene as a building block for organic solid state laser dyes: smaller energy gaps and enhanced stability. J Mater Chem C 9(12):4112–4118
Lin B et al (2018) A naphthalene-based fluorescent probe with a large Stokes shift for mitochondrial pH imaging. Analyst 143(20):5054–5060
[PMID:
30238115]
Uthuman A, Jayasinghe C, Fernando A (2019) Acute intravascular hemolysis due to naphthalene toxicity: a case report. J Med Case Rep 13(1):1–3
Lair A et al (2008) Naphthalene degradation in water by heterogeneous photocatalysis: an investigation of the influence of inorganic anions. J Photochem Photobiol A 193(2–3):193–203
Jing M et al (2020) Catalase and superoxide dismutase response and the underlying molecular mechanism for naphthalene. Sci Total Environ 736:139567
[PMID:
32479957]
Bunce NJ et al (1997) Reaction of naphthalene and its derivatives with hydroxyl radicals in the gas phase. Environ Sci Technol 31(8):2252–2259
Rahman MM et al (2012) Severe haemolytic anaemia due to ingestion of naphthalene (mothball) containing coconut oil. J Coll Physicians Surg Pak 22(11):740–741
[PMID:
23146862]
Carratt SA et al (2019) Metabolism and lung toxicity of inhaled naphthalene: Effects of postnatal age and sex. Toxicol Sci 170(2):536–548
[PMID:
31020322]
Batterman S et al (2012) Sources, concentrations, and risks of naphthalene in indoor and outdoor air. Indoor Air 22(4):266–278
[PMID:
22145682]
Preuss R, Angerer J, Drexler H (2003) Naphthalene—an environmental and occupational toxicant. Int Arch Occup Environ Health 76(8):556–576
[PMID:
12920524]
Yost EE et al (2021) Health effects of naphthalene exposure: A systematic evidence map and analysis of potential considerations for dose-response evaluation. Environ Health Perspect 129(7):076002
[PMID:
34251878]
Lu R et al (2005) Naphthalene distributions and human exposure in Southern California. Atmos Environ 39(3):489–507
Ahmad R, Amir SH, Khan SA (2020) Naphthalene mothballs poisoning leading to intravascular hemolysis: a case report. J Emerg Med 58(1):e1–e3
[PMID:
31744706]
Stohs SJ, Ohia S, Bagchi D (2002) Naphthalene toxicity and antioxidant nutrients. Toxicology 180(1):97–105
[PMID:
12324202]
Buckpitt A et al (2002) Naphthalene-induced respiratory tract toxicity: metabolic mechanisms of toxicity. Drug Metab Rev 34(4):791–820
[PMID:
12487150]
Wilson AS et al (1996) Characterisation of the toxic metabolite (s) of naphthalene. Toxicology 114(3):233–242
[PMID:
8980712]
Jafari A et al (2020) Sulfur and nitrogen doped-titanium dioxide coated on glass microspheres as a high performance catalyst for removal of naphthalene (C10H8) from aqueous environments using photo oxidation in the presence of visible and sunlight. Desalin Water Treat 192:195–212
Volney G et al (2018) Naphthalene toxicity: methemoglobinemia and acute intravascular hemolysis. Cureus 10(8)
Schreiner C (2003) Genetic toxicity of naphthalene: a review. J Toxicol Environ Health Part B 6(2):161–183
Kovalchuk N et al (2017) Impact of hepatic P450-mediated biotransformation on the disposition and respiratory tract toxicity of inhaled naphthalene. Toxicol Appl Pharmacol 329:1–8
[PMID:
28527914]
Nayak S, Patnaik L (2021) Role of Integrated biomarker response tool for assessment of naphthalene toxicity in anabas testudineus. Bull Environ Contam Toxicol 106(4):568–574
[PMID:
33420802]
Pirota V et al (2019) Naphthalene diimides as multimodal G-quadruplex-selective ligands. Molecules 24(3):426
[PMID:
30682828]
Jiang W-N et al (2021) CuI-mediated benzannulation of (ortho-arylethynyl) phenylenaminones to assemble α-aminonaphthalene derivatives. Org Chem Front
Li X-M et al (2021) Antibacterial naphthalene derivatives from the fermentation products of the endophytic fungus phomopsis fukushii. Chem Nat Compd 57(2):293–296
Merabet D (2018) Treatment of produced water by induced air flotation: effect of both TWEEN 80 and ethanol concentrations on the recovery of PAHs. Nova Biotechnol Chim 17(2):181–192
Javed M et al (2021) Optoelectronic properties of naphthalene bis-benzimidazole based derivatives and their photovoltaic applications. Comput Theor Chem 1204:113373
Kumari N et al (2020) Facile synthesis of naphthalene diimide (NDI) derivatives: aggregation-induced emission, photophysical and transport properties. J Mater Sci Mater Electron 31(5):4310–4322
Bhosale SV, Jani CH, Langford SJ (2008) Chemistry of naphthalene diimides. Chem Soc Rev 37(2):331–342
[PMID:
18197349]
Kumar VB et al (2021) The photophysical properties of naphthalene bridged disilanes. RSC Adv 11(35):21343–21350
[PMID:
35478807]
Mukherjee A, Ghosh S (2021) Core-substituted naphthalene-diimides (cNDI) and related derivatives: Versatile scaffold for supramolecular assembly and functional materials. Org Mater (AAM)
Zaier R, Ayachi S (2021) Toward designing new cyclopentadithiophene-naphthalene derivatives based small molecules for organic electronic applications: A theoretical investigation. Mater Today Commun 27:102370
An JM, Kim SH, Kim D (2020) Recent advances in two-photon absorbing probes based on a functionalized dipolar naphthalene platform. Org Biomol Chem 18(23):4288–4297
Ayranci E, Duman O (2010) Structural effects on the interactions of benzene and naphthalene sulfonates with activated carbon cloth during adsorption from aqueous solutions. Chem Eng J 156(1):70–76
Hashemi SH, Kaykhaii M (2017) Developments in methods of analysis for naphthalene sulfonates. Crit Rev Anal Chem 47(2):127–137
[PMID:
27541207]
Kameda T, Saito M, Umetsu Y (2006) Preparation and characterisation of Mg–Al layered double hydroxides intercalated with 2-naphthalene sulphonate and 2, 6-naphthalene disulphonate. Mater Trans 47(3):923–930
Jia M et al (2021) Investigation on the construction, photophysical properties and dyeing mechanism of 1, 8-naphthalimide-based fluorescent dyes suitable for dyeing wool fibers in supercritical CO2. Dyes Pigm 190:109343
Qian X et al (2010) “Alive” dyes as fluorescent sensors: fluorophore, mechanism, receptor and images in living cells. Chem Commun 46(35):6418–6436
Bekere L et al (2013) Synthesis and spectroscopic properties of 4-amino-1, 8-naphthalimide derivatives involving the carboxylic group: a new molecular probe for ZnO nanoparticles with unusual fluorescence features. Beilstein J Org Chem 9(1):1311–1318
[PMID:
23843926]
Belova A et al (2021) Solvent-controlled intramolecular excimer emission from organosilicon derivatives of naphthalene. Tetrahedron 93:132287
Erdemir S, Kocyigit O (2016) Anthracene excimer-based “turn on” fluorescent sensor for Cr3+ and Fe3+ ions: Its application to living cells. Talanta 158:63–69
[PMID:
27343579]
Cao J et al (2016) A ternary sensor system based on pyrene derivative-SDS assemblies-Cu2+ displaying dual responsive signals for fast detection of arginine and lysine in aqueous solution. J Photochem Photobiol A 314:66–74
Zhu Z, Li W, Yang C (2016) Switching monomer/excimer ratiometric fluorescence to time-resolved excimer probe for DNA detection: A simple strategy to enhance the sensitivity. Sens Actuators B Chem 224:31–36
Zhang Q et al (2015) Cyclodextrin supramolecular inclusion-enhanced pyrene excimer switching for time-resolved fluorescence detection of biothiols in serum. Biosens Bioelectron 68:253–258
[PMID:
25590970]
Yang M et al (2016) Polycation-induced benzoperylene probe excimer formation and the ratiometric detection of heparin and heparinase. Biosens Bioelectron 75:404–410
[PMID:
26344903]
Long S et al (2019) Rapid identification of bacteria by membrane-responsive aggregation of a pyrene derivative. ACS sensors 4(2):281–285
[PMID:
30672274]
Vollbrecht J (2018) Excimers in organic electronics. New J Chem 42(14):11249–11254
Thirion D et al (2012) Intramolecular excimer emission as a blue light source in fluorescent organic light emitting diodes: a promising molecular design. J Mater Chem 22(15):7149–7157
Suwara J et al (2020) Highly fluorescent distyrylnaphthalene derivatives as a tool for visualization of cellular membranes. Materials 13. https://doi.org/10.3390/ma13040951
Aladekomo J, Birks J (1965) ‘Excimer’ fluorescence VII. Spectral studies of naphthalene and its derivatives. Proc R Soc London Ser A Math Phys Sci 284(1399):551–565
Seixas de Melo J et al (2003) Energetics and dynamics of naphthalene polyaminic derivatives. Influence of structural design in the balance static vs dynamic excimer formation. J Phys Chem A 107(51):11307–11318
Adhikari S et al (2015) Sn(II) induced concentration dependent dynamic to static excimer conversion of a conjugated naphthalene derivative. Dalton Trans 44(32):14388–14393
[PMID:
26201049]
Hoche J et al (2017) The mechanism of excimer formation: an experimental and theoretical study on the pyrene dimer. Phys Chem Chem Phys 19(36):25002–25015
[PMID:
28876005]
Narayan B et al (2018) The effect of regioisomerism on the photophysical properties of alkylated-naphthalene liquids. Phys Chem Chem Phys 20(5):2970–2975
[PMID:
28952630]
Birajdar SS et al (2021) Conjoint use of naphthalene diimide and fullerene derivatives to generate organic semiconductors for n–type organic thin film transistors. ChemistryOpen 10(4):414–420
[PMID:
33543836]
Jang E et al (2018) Investigation of photophysical properties of 1, 8-naphthalimides with an extended conjugation on naphthalene moiety via Suzuki coupling reaction. J Photochem Photobiol A 364:145–150
Feng J et al (2011) Naphthalene-based fluorophores: Synthesis characterization, and photophysical properties. J Lumin 131(12):2775–2783
Maeda H, Maeda T, Mizuno K (2012) Absorption and fluorescence spectroscopic properties of 1-and 1, 4-silyl-substituted naphthalene derivatives. Molecules 17(5):5108–5125
[PMID:
22555299]
Dutta GK et al (2019) Aggregation behavior in naphthalene-appended diketopyrrolopyrrole derivatives and its gas adsorption impact on surface potential. J Mater Chem C 7(32):9954–9965
Panahi F et al (2021) A novel donor–π–acceptor halochromic 2, 6-distyrylnaphthalene chromophore: Synthesis, photophysical properties and DFT studies. RSC Adv 11(1):168–176
Krishnaveni K et al (2021) Selective anions mediated fluorescence “turn-on”, aggregation induced emission (AIE) and lysozyme targeting properties of pyrene-naphthalene sulphonyl conjugate. Spectrochim Acta Part A Mol Biomol Spectrosc 252:119537
Yang F et al (2012) Structure–property relationship of naphthalene based donor–π–acceptor organic dyes for dye-sensitized solar cells: remarkable improvement of open-circuit photovoltage. J Mater Chem 22(42):22550–22557
Chen W et al (2019) Facile synthesis of simple arylamine-substituted naphthalene derivatives as hole-transporting materials for efficient and stable perovskite solar cells. J Power Sources 425:87–93
Hachiya S, Asai K, Konishi G-I (2013) Unique solvent-dependent fluorescence of nitro-group-containing naphthalene derivatives with weak donor–strong acceptor system. Tetrahedron Lett 54(14):1839–1841
Gurusamy S et al (2021) Multiple target detection and binding properties of naphthalene-derived Schiff-base chemosensor. J Mol Liq 325:115190
Zhang W et al (2018) A novel naphthalene-based fluorescent probe for highly selective detection of cysteine with a large Stokes shift and its application in bioimaging. New J Chem 42(22):18109–18116
Al-Wattar A, Lumb M (1971) On the interpretation of iso-emissive points. Chem Phys Lett 8(4):331–336
Wang L et al (2021) Hg2+-induced excimer of a naphthalene-based fluorescent probe for recognition I–. Inorg Chem Commun 129:108662
Banerjee A et al (2012) Nickel (II)-induced excimer formation of a naphthalene-based fluorescent probe for living cell imaging. Inorg Chem 51(10):5699–5704
[PMID:
22559225]
Mallick S, Pal K, Koner AL (2016) Probing microenvironment of micelle and albumin using diethyl 6-(dimethylamino) naphthalene-2, 3-dicarboxylate: An electroneutral solvatochromic fluorescent probe. J Colloid Interface Sci 467:81–89
[PMID:
26773610]
Pandeeswar M, Govindaraju T (2013) Green-fluorescent naphthalene diimide: conducting layered hierarchical 2D nanosheets and reversible probe for detection of aromatic solvents. RSC Adv 3(29):11459–11462
