- Research works
- 107 ▲ 132% vs 2013–17
- Citations
- 2.5k 23.0 per fractional work
- Top-10% rate
- 22.5% record average 16.5%
- Open access
- 74% world 28%
Not ranked overall: ORFEO-CINQA Research Network is under the volume floor below which an excellence rate is noise. Not ranked is not the same as ranked last.
What does ORFEO-CINQA Research Network specialise in?
Where its research is concentrated relative to its size: Organic Chemistry takes 80.5× the share of its output that it takes of world research.
- Organic ChemistrySubfield · 26.8 works81×
- ChemistryField · 32.7 works47×
Location quotient, a volume reading rather than an impact one. It surfaces small, lopsided specialities.
Field profile
Location quotient across every field it publishes in: outside the ring is more than an institution of this size would be expected to publish, inside it is less.
Rings at 0.5×, 1× and 2×. Widest outward: Chemistry, 47.2×. Every wedge is a field page.
Which keywords describe research at ORFEO-CINQA Research Network?
By fractional works in 2022–2025, weighted toward what it does more of than the world: Catalysis, Organic Synthesis, Transition Metal Complexes, Transition Metal Catalysis, Medicinal Chemistry, Metal-Catalyzed Reactions, Oxidative Coupling and Heterocycles.
- Density Functional Theory
- Carbene Chemistry
- Green Chemistry
- Alcohol Activation
- Metal-Free Hydrogen Activation
- Catalytic
- Transition-Metal-Catalyzed
- Enantioselective
- Organometallic Chemistry
- Visible Light Photoredox Catalysis
- Enantioselective Reactions
- Asymmetric Synthesis
- C–H Activation
- Carbon–Carbon Bond Formation
- Enantioselective Synthesis
- Hydrogenation
- Heterocycles
- Metal-Catalyzed Reactions
- Transition Metal Catalysis
- Organic Synthesis
- Catalysis
- Transition Metal Complexes
- Medicinal Chemistry
- Oxidative Coupling
- Electrocatalysis
- Aryl Halides
- C-C Bond Formation
- Chiral Ligands
- Drug Design
- Electrochemical Methods
- Organocatalysis
- Homogeneous Catalysis
- Synthesis
- Sulfur Bond Formation
- Asymmetric Catalysis
- Frustrated Lewis Pairs
- Polymerization
- Dehydrogenation
- Hydrogen Bonding
- Cyclopropanation
Size is fractional works in 2022–2025 in the topics tagged with each word; colour is the word's share of this institution's work against its share of the world's. The 40 words are chosen for being large and distinctive. Each links to the topic it comes from most.
All 40 words, with their numbers
- Catalysis8▲ 28×17 topics
- Organic Synthesis8▲ 160×8 topics
- Transition Metal Complexes7▲ 186×4 topics
- Transition Metal Catalysis7▲ 186×4 topics
- Medicinal Chemistry6▲ 52×8 topics
- Metal-Catalyzed Reactions5▲ 197×3 topics
- Oxidative Coupling5▲ 223×2 topics
- Heterocycles5▲ 113×4 topics
- Electrocatalysis4▲ 33×4 topics
- Hydrogenation4▲ 53×4 topics
- Aryl Halides4▲ 217×2 topics
- Enantioselective Synthesis4▲ 142×6 topics
- C-C Bond Formation4▲ 197×3 topics
- Carbon–Carbon Bond Formation3▲ 177×1 topic
- Chiral Ligands3▲ 242×2 topics
- C–H Activation3▲ 177×1 topic
- Drug Design3▲ 121×3 topics
- Asymmetric Synthesis3▲ 137×6 topics
- Electrochemical Methods3▲ 278×1 topic
- Enantioselective Reactions3▲ 187×2 topics
- Organocatalysis3▲ 308×3 topics
- Visible Light Photoredox Catalysis3▲ 278×1 topic
- Homogeneous Catalysis3▲ 361×2 topics
- Organometallic Chemistry3▲ 152×4 topics
- Synthesis3▲ 18×10 topics
- Enantioselective3▲ 245×3 topics
- Sulfur Bond Formation3▲ 284×1 topic
- Transition-Metal-Catalyzed3▲ 284×1 topic
- Asymmetric Catalysis2▲ 148×3 topics
- Catalytic2▲ 40×4 topics
- Frustrated Lewis Pairs2▲ 408×1 topic
- Metal-Free Hydrogen Activation2▲ 408×1 topic
- Polymerization2▲ 47×2 topics
- Alcohol Activation2▲ 167×1 topic
- Dehydrogenation2▲ 66×1 topic
- Green Chemistry2▲ 24×7 topics
- Hydrogen Bonding2▲ 49×3 topics
- Carbene Chemistry2▲ 302×1 topic
- Cyclopropanation2▲ 302×1 topic
- Density Functional Theory2▲ 34×3 topics
Which research topics does ORFEO-CINQA Research Network publish most on?
By volume in 2022–2025: Catalytic C–H Functionalization Methods, Radical Photochemical Reactions, Sulfur-Based Synthesis Techniques and Organoboron and organosilicon chemistry.
Area is fractional works; colour is the subfield each topic belongs to.
- 1 Catalytic C–H Functionalization Methods Organic Chemistry 3 works
- 2 Radical Photochemical Reactions Organic Chemistry 3 works
- 3 Sulfur-Based Synthesis Techniques Organic Chemistry 3 works
- 4 Organoboron and organosilicon chemistry Organic Chemistry 2 works
- 5 Asymmetric Hydrogenation and Catalysis Inorganic Chemistry 2 works
- 6 Cyclopropane Reaction Mechanisms Organic Chemistry 2 works
- 7 Organometallic Complex Synthesis and Catalysis Organic Chemistry 1 works
- 8 Axial and Atropisomeric Chirality Synthesis Organic Chemistry 1 works
- 9 Fluorine in Organic Chemistry Pharmaceutical Science 1 works
- 10 Asymmetric Synthesis and Catalysis Organic Chemistry 1 works
How open and international is its research?
Against the world’s own shares — the tick on each track. Both are shares of its output, so they sit on one scale and can be read against each other as well as against the world.
World: 28% of research is openly available.
World: 19% is written across borders.
How has ORFEO-CINQA Research Network's research output changed?
Output in 2018–2022 was 132% higher than in 2013–2017.
The same series as a ribbon — one cell per year, darker for more. The line above answers how much; this answers when.
Other research institutions in Madrid
- Universidad Complutense de Madrid
- Universidad Autónoma de Madrid
- Universidad Politécnica de Madrid
- Consejo Superior de Investigaciones Científicas
- Universidad Carlos III de Madrid
- Universidad Rey Juan Carlos
- Universidad Nacional de Educación a Distancia
- Hospital Universitario La Paz
Research measures only: rankings here say nothing about teaching, admissions or student experience. Comparable institutions and collaboration partners are in the interactive view on the map.