Research graph
References from 1,5-Diaminonaphtalene is a Highly Performing Electron-Transfer Secondary-Reaction Matrix for Laser Desorption Ionization Mass Spectrometry of Indolenine-Based Croconaines. Local targets link to admitted publications; unresolved targets remain external evidence.
New Aromatic Anions. IV. Vibrational Spectra and Force Constants for C4O4-2 and C5O5-2
10.1021/ja00900a011 · 1963 · External reference
Soluble, infrared-absorbing croconate dyes from 2,6-di-tert-butyl-4- methylchalcogenopyrylium salts
10.1021/jo9916939 · 2000 · External reference
Infrared absorbing croconaine dyes: Synthesis and metal ion binding properties
10.1021/jo702209a · 2008 · External reference
Near-infrared squarate and croconate dianions derived from tetranitrofluorene
10.1039/c2nj40303j · 2012 · External reference
Synthesis and Computational Study of Semicroconaines and non-Symmetric Croconaines
10.1021/acs.joc.8b01930 · 2018 · External reference
Synthesis and Spectroscopic Characterization of New NIR Absorbing (2-Thienyl)- and (4-Dialkylaminoaryl)-substituted Croconic Acid Dyes
10.1002/jlac.1993199301149 · 1993 · External reference
Characterisation of new norcyanine dyes and their application as pH chromoionophores in optical sensors
10.1016/j.dyepig.2006.01.006 · 2007 · External reference
Croconaine Dyes – the Lesser Known Siblings of Squaraines
10.1002/ejoc.201700218 · 2017 · External reference
Activated photothermal heating using croconaine dyes
10.1039/c3sc51978c · 2013 · External reference
Croconaine rotaxane for acid activated photothermal heating and ratiometric photoacoustic imaging of acidic pH
10.1039/c5cc08317f · 2016 · External reference
Syntheses and some properties of infrared-absorbing croconium and related dyes
10.1016/0143-7208(89)85036-3 · 1989 · External reference
Selective photothermal inactivation of cells labeled with near-infrared croconaine dye
10.1039/c7cc05196d · 2017 · External reference
A highly sensitive and selective naked-eye probe for detection of Fe3+based on a 2,5-bis[3-benzyl-2-methylbenzothiazole]-croconaine
10.1016/j.tet.2017.01.049 · 2017 · External reference
Dual colorimetric and fluorescent chemosensor of Fe3+and Cu2+based on 2,5-bis[(4-carboxylic-piperidylamino)thiophenyl]-croconine
10.1016/j.tet.2015.06.081 · 2015 · External reference
Croconamides: a new dual hydrogen bond donating motif for anion recognition and organocatalysis
10.1039/c7ob00441a · 2017 · External reference
Resonant third-order optical nonlinearities of 1,3-bis[(3,3-dimethylindolin-2-ylidene)methyl]croconine
10.1016/j.physb.2006.02.022 · 2006 · External reference
Croconaines as molecular materials for organic electronics: synthesis, solid state structure and use in transistor devices
10.1039/c6tc00264a · 2016 · External reference
Croconaine nanoparticles with enhanced tumor accumulation for multimodality cancer theranostics
10.1016/j.biomaterials.2017.03.009 · 2017 · External reference
10.1002/9783527335961
10.1002/9783527335961 · 2013 · External reference
MALDI matrices for low molecular weight compounds: an endless story?
10.1007/s00216-018-1014-x · 2018 · External reference
Improvement of chlorophyll identification in foodstuffs by MALDI ToF/ToF mass spectrometry using 1,5-diaminonaphthalene electron transfer secondary reaction matrix
10.1007/s00216-015-8728-9 · 2015 · External reference
Electron-Transfer Secondary Reaction Matrices for MALDI MS Analysis of Bacteriochlorophyll a in Rhodobacter sphaeroides and Its Zinc and Copper Analogue Pigments
10.1007/s13361-016-1514-x · 2017 · External reference
4-Chloro-α-cyanocinnamic acid is an efficient soft matrix for cyanocobalamin detection in foodstuffs by matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS)
10.1002/jms.3817 · 2016 · External reference
9-Aminoacridine as a matrix for negative mode matrix-assisted laser desorption/ionization
10.1002/rcm.750 · 2002 · External reference
Characterization of various analytes using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and 2-[(2E)-3-(4-tert- butylphenyl)-2-methylprop-2-enylidene]malononitrile matrix
10.1021/ac050732f · 2006 · External reference
Ionization potential, electron affinity, electronegativity, hardness, and electron excitation energy: Molecular properties from density functional theory orbital energies
10.1021/jp0225774 · 2003 · External reference
Electrochemical bandgaps of substituted polythiophenes
10.1039/b301403g · 2003 · External reference
Electron Transfer Reactions in Laser Desorption/Ionization and Matrix-Assisted Laser Desorption/Ionization: Factors Influencing Matrix and Analyte Ion Intensities
10.1255/ejms.820 · 2006 · External reference
Photoionization pathways and free electrons in UV-MALDI
10.1021/ac035501s · 2004 · External reference
MALDI ionization: The role of in-plume processes
10.1021/cr0103773 · 2003 · External reference
The use of 2-[(2E)-3-(4-Tert-Butylphenyl)-2-Methylprop-2-enylidene]malononitrile as a matrix for matrix-assisted laser desorption/ionization mass spectrometry
10.1255/ejms.329 · 2000 · External reference
Photoelectron Spectroscopy ofperi-Amino Naphthalenes
10.1002/hlca.19740570405 · 1974 · External reference
Unresolved reference
2005 · External reference
Characterization of switched direct current gas sampling glow discharge ionization source for the time-of-flight mass spectrometer
10.1039/a906210f · 2000 · External reference
Plasma-source mass spectrometry for speciation analysis: State-of-the-art
10.1016/s0021-9673(04)01309-3 · 2004 · External reference
Ionization potential, electron affinity, electronegativity, hardness, and electron excitation energy: Molecular properties from density functional theory orbital energies
10.1021/jp0225774 · 2003 · External reference
Electron Transfer Reactivity in Matrix-Assisted Laser Desorption/Ionization (MALDI): Ionization Energy, Electron Affinity and Performance of the DCTB Matrix within the Thermochemical Framework
10.1021/jp060568f · 2006 · External reference
