Synthesis evidence

Tailoring Li-ion Storage and Transport in Two-Dimensional Conjugated Metal-Organic Frameworks via Precise Nitrogen Incorporation

Li X., Shi S., Cui F. et al. · Advanced Functional Materials · 2026 · e76160

7 structured synthesis routes

Completeness describes how fully the route could be reconstructed from the main article and supporting information.

Complete recipeSource: Both

Route 1: Solvothermal

13 · Synthesis of Cu-N2-OHBA · Scheme S3

Show 6 structured reagent records
RoleReagentAmount / concentrationSource
LinkerN2-OHBA15.2 mg, 0.03 mmol13 · Synthesis of Cu-N2-OHBA · Scheme S3
Solventdegassed N,N-dimethylformamide (DMF)1 mL13 · Synthesis of Cu-N2-OHBA · Scheme S3
Metal SourceCu(NO3)2.3H2O18.2 mg, 0.075 mmol13 · Synthesis of Cu-N2-OHBA · Scheme S3
SolventH2O2 mL13 · Synthesis of Cu-N2-OHBA · Scheme S3
SolventDI H2O150 mL x 213 · Synthesis of Cu-N2-OHBA · Scheme S3
Solventacetone15 mL x 213 · Synthesis of Cu-N2-OHBA · Scheme S3
Complete recipeSource: SI

Route 2: Drop Cast

42 · 6.1. Electrode preparation

Show 5 structured reagent records
RoleReagentAmount / concentrationSource
Othercarbon paper HCP020P1.5 x 1 cm strips42 · 6.1. Electrode preparation
OtherCu-N4-OHBA24 mg42 · 6.1. Electrode preparation
AdditiveSuper P3 mg42 · 6.1. Electrode preparation
OtherPTFE aqueous suspension3 mg · 30 wt%42 · 6.1. Electrode preparation
Solventethanol1 mL42 · 6.1. Electrode preparation
Complete recipeSource: Both

Route 3: Solvothermal

13 · Synthesis of Cu-N4-OHBA · Scheme S4

Show 6 structured reagent records
RoleReagentAmount / concentrationSource
LinkerN4-OHBA18.3 mg, 0.03 mmol13 · Synthesis of Cu-N4-OHBA · Scheme S4
Solventdegassed N,N-dimethylformamide (DMF)2 mL13 · Synthesis of Cu-N4-OHBA · Scheme S4
Metal SourceCu(NO3)2.3H2O18.2 mg, 0.075 mmol13 · Synthesis of Cu-N4-OHBA · Scheme S4
SolventH2O1 mL13 · Synthesis of Cu-N4-OHBA · Scheme S4
SolventDI H2O150 mL x 213 · Synthesis of Cu-N4-OHBA · Scheme S4
Solventacetone15 mL x 213 · Synthesis of Cu-N4-OHBA · Scheme S4
Complete recipeSource: SI

Route 4: Drop Cast

42 · 6.1. Electrode preparation

Show 5 structured reagent records
RoleReagentAmount / concentrationSource
Othercarbon paper HCP020P1.5 x 1 cm strips42 · 6.1. Electrode preparation
OtherCu-N2-OHBA24 mg42 · 6.1. Electrode preparation
AdditiveSuper P3 mg42 · 6.1. Electrode preparation
OtherPTFE aqueous suspension3 mg · 30 wt%42 · 6.1. Electrode preparation
Solventethanol1 mL42 · 6.1. Electrode preparation
Complete recipeSource: SI

Route 5: Other

14 · Activation of Cu-Nx-OHBA

Show 2 structured reagent records
RoleReagentAmount / concentrationSource
OtherCu-Nx-OHBA powdernot specified14 · Activation of Cu-Nx-OHBA
Solventacetone5 mL portions14 · Activation of Cu-Nx-OHBA
Complete recipeSource: SI

Route 6: Other

6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1

Show 11 structured reagent records
RoleReagentAmount / concentrationSource
Otherperchloropyrazine 11.0 g, 4.59 mmol6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
Other(3,4-dimethoxyphenyl)boronic acid 25.3 g, 29.0 mmol6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
AdditivePd(PPh3)4580 mg, 0.5 mmol6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
BaseK2CO3 aqueous solution27 mL · 2.0 M6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
Solventdeoxygenated dimethoxyethane (DME)60 mL6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
OxidantFeCl32.6 g6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
Solventnitromethane20 mL6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
Solventanhydrous chloroform60 mL6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
OtherBBr3 in dichloromethane60.0 mL · 1.0 M6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
Otherdegassed anhydrous MeOH50 mL6 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
Solventdegassed dichloromethane100 mL x 36 · 2.2. Synthesis of N2-OHBA ligand · Scheme S1
Partial recipeSource: SI

Route 7: Other

10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2

Show 9 structured reagent records
RoleReagentAmount / concentrationSource
Othercompound 5726 mg, 1.0 mmol10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2
OxidantFeCl32.0 g10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2
Solventnitromethane20 mL10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2
Solventanhydrous chloroform60 mL10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2
SolventMeOH100 mL x 310 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2
Othercompound 61.08 g, 1.5 mmol10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2
OtherBBr3 in DCM60 mL · 1.0 M10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2
Solventanhydrous dichloromethane40 mL10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2
Otherdegassed MeOH50 mL10 · 2.3. Synthesis of N4-OHBA ligand · Scheme S2