SASSI, MAURO
 Distribuzione geografica
Continente #
NA - Nord America 11.014
AS - Asia 6.725
EU - Europa 6.069
SA - Sud America 842
AF - Africa 144
OC - Oceania 14
Continente sconosciuto - Info sul continente non disponibili 5
Totale 24.813
Nazione #
US - Stati Uniti d'America 10.737
SG - Singapore 2.169
IT - Italia 1.583
CN - Cina 1.379
VN - Vietnam 1.257
DE - Germania 1.178
RU - Federazione Russa 751
HK - Hong Kong 722
BR - Brasile 629
SE - Svezia 494
IE - Irlanda 462
GB - Regno Unito 320
IN - India 289
FR - Francia 263
UA - Ucraina 228
CA - Canada 184
AT - Austria 165
KR - Corea 150
FI - Finlandia 137
BD - Bangladesh 118
ID - Indonesia 101
TR - Turchia 100
AR - Argentina 90
PL - Polonia 83
JP - Giappone 80
ES - Italia 71
NL - Olanda 61
MX - Messico 60
IQ - Iraq 57
DK - Danimarca 55
PK - Pakistan 53
ZA - Sudafrica 49
CH - Svizzera 45
CZ - Repubblica Ceca 42
BE - Belgio 38
SA - Arabia Saudita 31
CO - Colombia 28
PH - Filippine 27
UZ - Uzbekistan 27
TW - Taiwan 23
VE - Venezuela 23
LT - Lituania 20
AE - Emirati Arabi Uniti 19
EC - Ecuador 19
MA - Marocco 19
CL - Cile 18
IL - Israele 18
KE - Kenya 15
AU - Australia 13
MY - Malesia 13
RO - Romania 13
TN - Tunisia 13
EG - Egitto 10
IR - Iran 10
PY - Paraguay 10
UY - Uruguay 10
AL - Albania 9
AZ - Azerbaigian 9
BG - Bulgaria 9
ET - Etiopia 8
RS - Serbia 8
TH - Thailandia 8
DZ - Algeria 7
GR - Grecia 7
JO - Giordania 7
KZ - Kazakistan 7
PE - Perù 7
BO - Bolivia 6
GT - Guatemala 6
NP - Nepal 6
AM - Armenia 5
BH - Bahrain 5
CI - Costa d'Avorio 5
CR - Costa Rica 5
JM - Giamaica 5
LB - Libano 5
OM - Oman 5
AO - Angola 4
GE - Georgia 4
HN - Honduras 4
HU - Ungheria 4
PT - Portogallo 4
SK - Slovacchia (Repubblica Slovacca) 4
KG - Kirghizistan 3
LV - Lettonia 3
NI - Nicaragua 3
PA - Panama 3
PS - Palestinian Territory 3
SN - Senegal 3
XK - ???statistics.table.value.countryCode.XK??? 3
BN - Brunei Darussalam 2
BY - Bielorussia 2
CY - Cipro 2
DO - Repubblica Dominicana 2
HR - Croazia 2
LA - Repubblica Popolare Democratica del Laos 2
LY - Libia 2
MK - Macedonia 2
MM - Myanmar 2
MU - Mauritius 2
Totale 24.783
Città #
Ann Arbor 2.612
Singapore 1.340
Ashburn 971
Frankfurt am Main 747
Hong Kong 683
San Jose 641
Woodbridge 588
Milan 537
Fairfield 519
Chandler 495
Dublin 443
Ho Chi Minh City 371
Wilmington 359
Houston 343
Hanoi 253
New York 248
Beijing 233
Los Angeles 229
Seattle 217
Santa Clara 208
Jacksonville 193
Dallas 192
Dearborn 184
Cambridge 176
Chicago 158
Hefei 150
Vienna 140
Princeton 132
Munich 112
Shanghai 106
The Dalles 100
Seoul 99
Moscow 95
Council Bluffs 88
Dong Ket 87
Nanjing 78
Jakarta 72
Lauterbourg 71
Rome 70
Buffalo 67
Warsaw 61
São Paulo 60
Helsinki 53
Kent 52
Lawrence 52
Altamura 50
Toronto 49
Orem 46
Tokyo 45
San Diego 44
Da Nang 42
London 42
Stockholm 42
Haiphong 40
Montreal 40
Turin 39
Brussels 38
Bologna 35
Brno 33
Guangzhou 33
Florence 32
Lachine 32
Denver 31
Turku 31
Atlanta 30
Fremont 29
Naples 29
Chennai 27
Manchester 27
Brooklyn 26
Johannesburg 26
Nanchang 26
Poplar 26
Pune 26
Zurich 26
Baghdad 25
Hebei 25
Amsterdam 24
Andover 23
Biên Hòa 23
Mumbai 23
Can Tho 22
Rio de Janeiro 22
Tashkent 22
Boardman 21
Lahore 21
Nuremberg 20
Tianjin 20
Boston 19
Ankara 18
Changsha 18
Desio 18
Dhaka 18
Hangzhou 17
Jinan 17
Lappeenranta 17
Thái Nguyên 17
Mexico City 16
Phoenix 16
Quận Bình Thạnh 16
Totale 16.225
Nome #
New Roll-to-Roll Processable PEDOT-Based Polymer with Colorless Bleached State for Flexible Electrochromic Devices 582
Efficient, fast and reabsorption-free perovskite nanocrystal-based sensitized plastic scintillators 571
Thermochromic Latent-Pigment-Based Time–Temperature Indicators for Perishable Goods 559
State-of-the-Art Neutral Tint Multichromophoric Polymers for High-Contrast See-Through Electrochromic Devices 536
Suzuki-Miyaura Micellar One-Pot Synthesis of Symmetrical and Unsymmetrical 4,7-Diaryl-5,6-difluoro-2,1,3-benzothiadiazole Luminescent Derivatives in Water and under Air 513
Sustainable Access to π-Conjugated Molecular Materials via Direct (Hetero)Arylation Reactions in Water and under Air 489
Chemically Sustainable Large Stokes Shift Derivatives for High-Performance Large-Area Transparent Luminescent Solar Concentrators 489
Efficient synthesis of organic semiconductors by Suzuki-Miyaura coupling in an aromatic micellar medium 485
Triplet-triplet annihilation based photon up-conversion in hybrid molecule-semiconductor nanocrystal systems 477
Synthesis of conjugated polymers by sustainable Suzuki polycondensation in water and under aerobic conditions 451
Multichromophoric Electrochromic Polymers toward High Contrast Neutral Tint See-Through Electrochromic Devices 433
First demonstration of the use of very large Stokes shift cycloparaphenylenes as promising organic luminophores for transparent luminescent solar concentrators 425
Preparation of Naphthalene Dianhydride Bithiophene Copolymers by Direct Arylation Polycondensation and the Latent Pigment Approach 408
Suzuki-Miyaura Micellar Cross-Coupling in Water, at Room Temperature, and under Aerobic Atmosphere 406
Synthesis of Fluorinated Acridines via Sequential Micellar Buchwald-Hartwig Amination/Cyclization of Aryl Bromides 403
High Stokes shift perylene dyes for luminescent solar concentrators 377
Straightforward, Sustainable, and Scalable Access to 3,4-Perylenedicarboxylic Monoanhydride 369
Suzuki-Miyaura cross-coupling of latent pigments in water/toluene emulsion under aerobic atmosphere 360
Stokes shift/emission efficiency trade-off in donor-acceptor perylenemonoimides for luminescent solar concentrators 357
Polyconjugated materials for printed (opto)electronics: introducing sustainability 356
Taming troublesome suzuki-miyaura reactions in water solution of surfactants by the use of lecithin: A step beyond the micellar model 341
Application of micellar catalysis for a greener synthesis of Iopamidol 337
Heterocycle-based redox active, electrochromic organic materials 335
Exomethylene-3,4-ethylenedioxythiophene (emEDOT): A new versatile building block for functionalized electropolymerized poly(3,4-ethylenedioxythiophenes) (PEDOTs) 325
Post-deposition Activation of Latent Hydrogen-Bonding: A New Paradigm for Enhancing the Performances of Bulk Heterojunction Solar Cells 320
First Demonstration of the Applicability of the Latent Pigment Approach to Plastic Luminescent Solar Concentrators 320
Synthesis and Characterization of Squaraine-Based Photocrosslinkable Resists for Bulk Heterojunction Solar Cells 315
Organic electrochromic materials having high transparency and high contrast in the visible range 308
Near-infrared roll-off-free electroluminescence from highly stable diketopyrrolopyrrole light emitting diodes 306
Open circuit voltage tuning through molecular design in hydrazone end capped donors for bulk heterojunction solar cells 304
Micellar catalysis beyond the hydrophobic effect: Efficient palladium catalyzed Suzuki-Miyaura coupling of water and organic solvent insoluble pigments with food grade surfactants 304
Latent hydrogen bond: a versatile tool enabling the facile preparation of organic devices 298
Sustainable synthesis of conjugated polymers by Suzuki-Miyaura in aqueous environment, and application of their waterborne dispersions 297
Self-Assembled Dual Dye-Doped Nanosized Micelles for High-Contrast Up-Conversion Bioimaging 296
Unexpected Enhancement of Molecular n-Doping Efficiency in Polymer Thin Films by a Degradation Product 288
A latent pigment strategy for robust active layers in solution-processed, complementary organic field-effect transistors 286
An efficient Buchwald–Hartwig amination protocol enables the synthesis of new branched and polymeric hole transport materials for perovskite solar cells 284
Straightforward fabrication of stable white LEDs by embedding of inorganic UV-LEDs into bulk polymerized polymethyl-methacrylate doped with organic dyes 283
Crosslinked Electroactive Polymers Containing Naphthalene-Bisimide Redox Centers for Energy Storage 278
Unraveling Triplet Excitons Photophysics in Hyper-Cross-Linked Polymeric Nanoparticles: Toward the Next Generation of Solid-State Upconverting Materials 273
Role played by chain length and polarity of n-substitutents in electrochromic polymers from the tri-heterocyclic monomer pyrrole-thiophene- pyrrole 271
Twists and turns around a square: The many faces of Squaraine chemistry 271
Sustainable, Efficient, and Scalable Preparation of Pure and Performing Spiro-OMeTAD for Perovskite Solar Cells 271
Ab Initio Simulations of Interfaces between SAM-Modified Gold Electrodes and n-Type or p-Type Organic Semiconductors Based on the Benzothieno-Benzothiophene (BTBT) Architecture 270
Sustainable access to π-conjugated molecular building blocks via phosphine-free, ppm palladium level Suzuki-Miyaura reaction in water 269
An Integrated theoretical/experimental study of quinolinic-isoquinolinic derivatives acting as reversible electrochromes 268
Gray to colorless switching, crosslinked electrochromic polymers with outstanding stability and transmissivity from naphthalenediimmide-functionalized EDOT 267
Tackling materials science with the tools of organic chemistry: dyes, pigments and all there is in between 264
Panchromatic cross-substituted squaraines for dye-sensitized solar cell applications 262
Investigation of redox activity in the napthalenediimide-poly(3,4- ethylenedioxythiophene) cross-linked polymers 260
Direct detection of molecular hydrogen upon p- and n-doping of organic semiconductors with complex oxidants or reductants 249
A High Molecular Weight Donor for Electron Injection Interlayers on Metal Electrodes 246
Organic Solvent Free Synthesis and Processing of Semiconducting Polymers for Field Effect Transistors in Waterborne Dispersions 245
The role of electrolyte ions on the electrochemical properties of thiophene based conducting polymers 244
Syntheses of Organic Semiconductors in Water. Recent Advancement in the Surfactants Enhanced Green Access to Polyconjugated Molecules 243
Front Cover: Preparation of Naphthalene Dianhydride Bithiophene Copolymers by Direct Arylation Polycondensation and the Latent Pigment Approach (ChemPlusChem 9/2019) 242
Selective photoredox direct arylations of aryl bromides in water in a microfluidic reactor 240
Process for the preparation of 2,4,6-triiodoisophthalic bisamides 232
Repurposing discarded porphyrin waste as electrocatalysts for the oxygen reduction reaction 231
Organic active materials for electrochemical energy storage 228
Perfluorinated nitrosopyrazolone-based erbium chelates: A new efficient solution processable NIR emitter 222
Latent pigments with extended conjugation. Resourceful materials for organic electronics. 221
High detectivity squaraine-based near infrared photodetector with nA/cm2 dark current 218
Transparent and Highly Responsive Phototransistors Based on a Solution-Processed, Nanometers-Thick Active Layer, Embedding a High-Mobility Electron-Transporting Polymer and a Hole-Trapping Molecule 218
High voltage organic materials for energy storage applications 211
Synergism in multicomponent self-propagating molecular assemblies 209
Understanding How to Control Efficiency of Benzimidazoline Based n-type Dopants: A Structural Approach 206
Organic Electrochromic Polymers: State-of-the-Art Neutral Tint Multichromophoric Polymers for High-Contrast See-Through Electrochromic Devices (Adv. Funct. Mater. 29/2016) 205
Multichromophoric electrochromic polymers: Colour tuning of conjugated polymers through the side chain functionalization approach 204
Molecule and electron transfer through coordination-based molecular assemblies 203
Synthesis and electrocatalytic activity of transition metal electrocatalysts for oxygen reduction reaction derived from porphyrins and their wastes 199
New organic active materials for energy storage with high capacity and high voltage 195
Optimization of electrochromic materials by molecular design: the Naphthalenediimide-Functionalized EDOT 194
First demonstration of the use of open-shell derivatives as organic luminophores for transparent luminescent solar concentrators 193
Synthesis of Molecular and Polymeric Benzimidazoline-based N-Type Dopants 192
Upcycling the discarded porphyrins wastes into electrocatalysts for oxygen reduction reaction 192
Luminescent persistent radicals for photon management applications 184
Understanding the Interplay Between Thermal Activation, Diffusion, and Phase Segregation of Molecular Dopants Blended with Polymeric Semiconductors 183
Diketopyrrolopyrrole latent pigment-based bilayer solar cells 182
A n-type, Stable Electrolyte Gated Organic Transistor Based on a Printed Polymer 181
Sustainable synthesis of conjugated polymers by Suzuki-Miyaura in aqueous environment, and application of their waterborne dispersions 176
Electrochromic Polymer Ink Derived from a Sidechain-Modified EDOT for Electrochromic Devices with Colorless Bright State 173
Sustainable synthetic methods for the production of perylenemonoimide derivatives and their application in retinal photosensitisation 158
Chitosan-gated organic transistors printed on ethyl cellulose as a versatile platform for edible electronics and bioelectronics 147
Challenging the Scope of Micellar Catalysis: Efficient Suzuki-Miyaura Couplings in Aqueous Dispersions 144
Synthesis of Dithienocyclohexanones (DTCHs) as a Family of Building Blocks for π-Conjugated Compounds in Organic Electronics 129
Hitchhiker’s Guide to the Preparation of Novel Benzimidazoline-Based n-Type Dopants 122
State of the Art in Flexible Electrochromic Devices for Shading Applications 92
Transparent neutral-colored CsPbBr3perovskite solar cell with biological soybean lecithin food additives 50
COLLOIDAL COATING DISPERSION 30
PROCESS FOR THE PREPARATION OF DISUBSTITUTED DIARYLOXYBENZOHETERODIAZOLE COMPOUNDS 24
Totale 25.474
Categoria #
all - tutte 73.478
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 73.478


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021432 0 0 0 0 0 0 0 0 0 0 142 290
2021/20222.140 215 202 199 182 91 169 133 217 129 163 190 250
2022/20232.347 268 655 266 237 173 262 39 126 130 44 75 72
2023/20241.574 68 47 80 76 185 370 286 105 116 40 60 141
2024/20254.122 189 376 346 266 280 231 245 163 405 600 360 661
2025/20268.801 1.320 711 705 1.099 1.060 481 1.376 441 774 819 15 0
Totale 25.474