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Célia Fonseca Guerra

Name	Célia Fonseca Guerra
Time	1995- (Wirkungsdaten)
Place	Leiden (Wirkungsort) Niederlande
Gender	weiblich
Academic degree	Dr.
Variant	Célia Fonseca Guerra
Related	Universiteit Leiden Vrije Universiteit Amsterdam
Source	Homepage: http://www.few.vu.nl/~guerra/ (Stand: 06.01.2023)
Record type	Person
GND-Identifier	1261085922
Record ID	1261085922
Involved in show all Synthesis, Reactivity, and Bonding Analysis of a Tetracoordinated Nickel Carbene Chalcogen Atom Size: A Key Parameter in Modulating Carbonyl Compound Properties Cooperativity in Hydrogen‐Bonded Macrocycles Derived from Nucleobases More Electropositive is More Electronegative: Atom Size Determines C=X Group Electronegativity Front Cover: Cooperativity in Hydrogen‐Bonded Macrocycles Derived from Nucleobases (Eur. J. Org. Chem. 19/2024) Blueshift in Trifurcated Hydrogen Bonds: A Tradeoff between Tetrel Bonding and Steric Repulsion Front Cover: Blueshift in Trifurcated Hydrogen Bonds: A Tradeoff between Tetrel Bonding and Steric Repulsion (ChemPhysChem 1/2024) Blueshift in Trifurcated Hydrogen Bonds: A Tradeoff between Tetrel Bonding and Steric Repulsion Chalcogen Atom Size Dictates Stability of Benzene‐1,3,5‐triamide Polymers: Overlooked Role of Geometrical Fit for Enhanced Hydrogen Bonding Understanding the influence of alkali cations and halogen anions on the cooperativity of cyclic hydrogen‐bonded rosettes in supramolecular stacks Redox Conversion of Cobalt (II)‐Diselenide to Cobalt (III)‐Selenolate Compounds: Comparison with Their Sulfur Analogs How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order Front Cover: B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order (ChemistryOpen 2/2022) σ‐Electrons Responsible for Cooperativity and Ring Equalization in Hydrogen‐Bonded Supramolecular Polymers σ‐Electrons Responsible for Cooperativity and Ring Equalization in Hydrogen‐Bonded Supramolecular Polymers σ‐Electrons Responsible for Cooperativity and Ring Equalization in Hydrogen‐Bonded Supramolecular Polymers How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes Boron Tunneling in the “Weak” Bond‐Stretch Isomerization of N−B Lewis Adducts Cooperative Self‐Assembly in Linear Chains Based on Halogen Bonds Cooperative Self‐Assembly in Linear ChainsBased on Halogen Bonds The Gauche Effect in XCH 2 CH 2 X Revisited How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes Front Cover: How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes (ChemPhysChem 22/2021) Nature of Alkali‐ and Coinage‐Metal Bonds versus Hydrogen Bonds Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length Evaluation of the Alicyclic Gauche Effect in 2‐Fluorocyclohexanone Analogs: a Combined NMR and DFT Study Effect of Alkali Metal Cations on Length and Strength of Hydrogen Bonds in DNA Base Pairs Nature and Strength of Lewis Acid/Base Interaction in Boron and Nitrogen Trihalides Front Cover: Nature and Strength of Lewis Acid/Base Interaction in Boron and Nitrogen Trihalides (Chem. Asian J. 23/2020) The Nature of Nonclassical Carbonyl Ligands Explained by Kohn–Sham Molecular Orbital Theory Distortion‐Controlled Redshift of Organic Dye Molecules Designing Self‐Assembled Rosettes: Why Ammeline is a Superior Building Block to Melamine Designing Self‐Assembled Rosettes: Why Ammeline is a Superior Building Block to Melamine Front Cover: Designing Self‐Assembled Rosettes: Why Ammeline is a Superior Building Block to Melamine (ChemistryOpen 2/2019) The Nature of Hydrogen Bonds: A Delineation of the Role of Different Energy Components on Hydrogen Bond Strengths and Lengths Front Cover: The Nature of Hydrogen Bonds: A Delineation of the Role of Different Energy Components on Hydrogen Bond Strengths and Lengths (Chem. Asian J. 16/2019) Supramolecular Self‐Sorting Networks using Hydrogen‐Bonding Motifs Cover Feature: Supramolecular Self‐Sorting Networks using Hydrogen‐Bonding Motifs (Chem. Eur. J. 3/2019) Integrative Theory/Experiment‐Driven Exploration of a Multicomponent Reaction towards Imidazoline‐2‐(thi) ones RNA versus DNA G‐Quadruplex: The Origin of Increased Stability Cover Feature: RNA versus DNA G‐Quadruplex: The Origin of Increased Stability (Chem. Eur. J. 61/2018) Mixed guanine, adenine base quartets: possible roles of protons and metal ions in their stabilization Alkali Metal Cation Affinities of Anionic Main Group‐Element Hydrides Across the Periodic Table Cover Feature: Alkali Metal Cation Affinities of Anionic Main Group‐Element Hydrides Across the Periodic Table (Chem. Asian J. 19/2017) Hydrogen‐Bond Strength of CC and GG Pairs Determined by Steric Repulsion: Electrostatics and Charge Transfer Overruled Hydrogen‐Bond Strength of CC and GG Pairs Determined by Steric Repulsion: Electrostatics and Charge Transfer Overruled Cover Picture: Hydrogen‐Bond Strength of CC and GG Pairs Determined by Steric Repulsion: Electrostatics and Charge Transfer Overruled (Chem. Eur. J. 43/2017) Cooperativity in the Self‐Assembly of the Guanine Nucleobase into Quartet and Ribbon Structures on Surfaces Inside Cover: Cooperativity in the Self‐Assembly of the Guanine Nucleobase into Quartet and Ribbon Structures on Surfaces (Chem. Eur. J. 13/2017) Enhanced π‐Back‐Donation as a Way to Higher Coordination Numbers in d 10 (M (NHC) n) Complexes: A DFT Study Source of Cooperativity in Halogen‐Bonded Haloamine Tetramers Inside Cover: Source of Cooperativity in Halogen‐Bonded Haloamine Tetramers (ChemPhysChem 4/2016) Alkali Metal Cation versus Proton and Methyl Cation Affinities: Structure and Bonding Mechanism Modified Guanines as Constituents of Smart Ligands for Nucleic Acid Quadruplexes

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Katalog der Deutschen Nationalbibliothek

Célia Fonseca Guerra

Synthesis, Reactivity, and Bonding Analysis of a Tetracoordinated Nickel Carbene

Chalcogen Atom Size: A Key Parameter in Modulating Carbonyl Compound Properties

Cooperativity in Hydrogen‐Bonded Macrocycles Derived from Nucleobases

More Electropositive is More Electronegative: Atom Size Determines C=X Group Electronegativity

Front Cover: Cooperativity in Hydrogen‐Bonded Macrocycles Derived from Nucleobases (Eur. J. Org. Chem. 19/2024)

Blueshift in Trifurcated Hydrogen Bonds: A Tradeoff between Tetrel Bonding and Steric Repulsion

Front Cover: Blueshift in Trifurcated Hydrogen Bonds: A Tradeoff between Tetrel Bonding and Steric Repulsion (ChemPhysChem 1/2024)

Blueshift in Trifurcated Hydrogen Bonds: A Tradeoff between Tetrel Bonding and Steric Repulsion

Chalcogen Atom Size Dictates Stability of Benzene‐1,3,5‐triamide Polymers: Overlooked Role of Geometrical Fit for Enhanced Hydrogen Bonding

Understanding the influence of alkali cations and halogen anions on the cooperativity of cyclic hydrogen‐bonded rosettes in supramolecular stacks

Redox Conversion of Cobalt (II)‐Diselenide to Cobalt (III)‐Selenolate Compounds: Comparison with Their Sulfur Analogs

How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides

How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides

How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides

B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order

B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order

Front Cover: B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order (ChemistryOpen 2/2022)

σ‐Electrons Responsible for Cooperativity and Ring Equalization in Hydrogen‐Bonded Supramolecular Polymers

σ‐Electrons Responsible for Cooperativity and Ring Equalization in Hydrogen‐Bonded Supramolecular Polymers

σ‐Electrons Responsible for Cooperativity and Ring Equalization in Hydrogen‐Bonded Supramolecular Polymers

How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes

Boron Tunneling in the “Weak” Bond‐Stretch Isomerization of N−B Lewis Adducts

Cooperative Self‐Assembly in Linear Chains Based on Halogen Bonds

Cooperative Self‐Assembly in Linear ChainsBased on Halogen Bonds

The Gauche Effect in XCH 2 CH 2 X Revisited

How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes

Front Cover: How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes (ChemPhysChem 22/2021)

Nature of Alkali‐ and Coinage‐Metal Bonds versus Hydrogen Bonds

Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length

Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length

Evaluation of the Alicyclic Gauche Effect in 2‐Fluorocyclohexanone Analogs: a Combined NMR and DFT Study

Effect of Alkali Metal Cations on Length and Strength of Hydrogen Bonds in DNA Base Pairs

Nature and Strength of Lewis Acid/Base Interaction in Boron and Nitrogen Trihalides

Front Cover: Nature and Strength of Lewis Acid/Base Interaction in Boron and Nitrogen Trihalides (Chem. Asian J. 23/2020)

The Nature of Nonclassical Carbonyl Ligands Explained by Kohn–Sham Molecular Orbital Theory

Distortion‐Controlled Redshift of Organic Dye Molecules

Designing Self‐Assembled Rosettes: Why Ammeline is a Superior Building Block to Melamine

Designing Self‐Assembled Rosettes: Why Ammeline is a Superior Building Block to Melamine

Front Cover: Designing Self‐Assembled Rosettes: Why Ammeline is a Superior Building Block to Melamine (ChemistryOpen 2/2019)

The Nature of Hydrogen Bonds: A Delineation of the Role of Different Energy Components on Hydrogen Bond Strengths and Lengths

Front Cover: The Nature of Hydrogen Bonds: A Delineation of the Role of Different Energy Components on Hydrogen Bond Strengths and Lengths (Chem. Asian J. 16/2019)

Supramolecular Self‐Sorting Networks using Hydrogen‐Bonding Motifs

Cover Feature: Supramolecular Self‐Sorting Networks using Hydrogen‐Bonding Motifs (Chem. Eur. J. 3/2019)

Integrative Theory/Experiment‐Driven Exploration of a Multicomponent Reaction towards Imidazoline‐2‐(thi) ones

RNA versus DNA G‐Quadruplex: The Origin of Increased Stability

Cover Feature: RNA versus DNA G‐Quadruplex: The Origin of Increased Stability (Chem. Eur. J. 61/2018)

Mixed guanine, adenine base quartets: possible roles of protons and metal ions in their stabilization

Alkali Metal Cation Affinities of Anionic Main Group‐Element Hydrides Across the Periodic Table

Cover Feature: Alkali Metal Cation Affinities of Anionic Main Group‐Element Hydrides Across the Periodic Table (Chem. Asian J. 19/2017)

Hydrogen‐Bond Strength of CC and GG Pairs Determined by Steric Repulsion: Electrostatics and Charge Transfer Overruled

Hydrogen‐Bond Strength of CC and GG Pairs Determined by Steric Repulsion: Electrostatics and Charge Transfer Overruled

Cover Picture: Hydrogen‐Bond Strength of CC and GG Pairs Determined by Steric Repulsion: Electrostatics and Charge Transfer Overruled (Chem. Eur. J. 43/2017)

Cooperativity in the Self‐Assembly of the Guanine Nucleobase into Quartet and Ribbon Structures on Surfaces

Inside Cover: Cooperativity in the Self‐Assembly of the Guanine Nucleobase into Quartet and Ribbon Structures on Surfaces (Chem. Eur. J. 13/2017)

Enhanced π‐Back‐Donation as a Way to Higher Coordination Numbers in d 10 (M (NHC) n) Complexes: A DFT Study

Source of Cooperativity in Halogen‐Bonded Haloamine Tetramers

Inside Cover: Source of Cooperativity in Halogen‐Bonded Haloamine Tetramers (ChemPhysChem 4/2016)

Alkali Metal Cation versus Proton and Methyl Cation Affinities: Structure and Bonding Mechanism

Modified Guanines as Constituents of Smart Ligands for Nucleic Acid Quadruplexes